UPS
MCID: UND005
MIFTS: 67

Undifferentiated Pleomorphic Sarcoma (UPS)

Categories: Bone diseases, Cancer diseases, Immune diseases, Rare diseases, Skin diseases

Aliases & Classifications for Undifferentiated Pleomorphic Sarcoma

MalaCards integrated aliases for Undifferentiated Pleomorphic Sarcoma:

Name: Undifferentiated Pleomorphic Sarcoma 52 58 6 17
Malignant Fibrous Histiocytoma 52 71
Ups 52 58
Malignant Fibrohistiocytic Tumors 52

Characteristics:

Orphanet epidemiological data:

58
undifferentiated pleomorphic sarcoma
Inheritance: Not applicable; Prevalence: 1-9/1000000 (Europe),1-9/1000000 (United States); Age of onset: Adolescent,Adult,Childhood,Elderly; Age of death: any age;

Classifications:

Orphanet: 58  
Rare bone diseases


External Ids:

MESH via Orphanet 44 D051677
ICD10 via Orphanet 33 C49.9
UMLS via Orphanet 72 C0334463
Orphanet 58 ORPHA2023
UMLS 71 C0334463

Summaries for Undifferentiated Pleomorphic Sarcoma

NIH Rare Diseases : 52 The following summary is from Orphanet , a European reference portal for information on rare diseases and orphan drugs. Orpha Number: 2023 Definition An aggressive sarcoma of soft tissues or bone that can arise from any part of the body, clinically presenting as swelling, mass, pain, pathological fracture and occasional systemic features and is characterized by high local recurrence and significant metastasis . Epidemiology UPS ranks the 4th most common soft tissue sarcoma with a slight male preponderance. The incidence has been evaluated to be close to 0.8-1 new case per 100000 per year in one European series. Clinical description The tumor arises most commonly during the sixth and seventh decades of life. The most common sites of involvement include lower extremities (mainly thigh) followed by upper arms, retroperitoneum, viscera, head and neck (in childhood). Primary osseous UPS most commonly occurs in distal femur, proximal tibia, proximal femur and humerus. Patients may present pain, swelling / mass and pathological fractures. In the skin, UPS presents as a relatively painless, rapidly enlarging nodule. Anorexia, malaise, fever and weight loss are present in retroperitoneal and inflammatory forms of UPS. Most UPS recur locally; distant metastases are common (the most frequent is lung). Regional metastases are rare. Etiology UPS is thought to be derived from a primitive mesenchymal cell capable of differentiating into histiocytes, fibroblasts , myofibroblasts and osteoclasts. The etiology of the tumor remains unknown. Prior radiation therapy is a likely risk factor in some cases. Diagnostic methods Any tumor mass over 5 cm is suspected to be a sarcoma. Magnetic resonance imaging (MRI) is the imaging method of choice for limbs and shows a high signal on T2 weighted images. Histology of biopsy specimen prior to any treatment is crucial to reach diagnosis and shows pleomorphic spindle cell population with large atypical cells frequently exhibiting numerous irregular mitotic figures, associated regions of hemorrhage and necrosis, associated lymphohistiocytic infiltrate and invasion of dermis. Immunohistochemical staining is negative for S-100, HMB-45, CD34 and cytokeratin which assists in ruling out other soft tissue tumors. Most cases previously diagnosed as malignant fibrous histiocytoma have been reclassified into other histological types of sarcoma. Differential diagnosis When occurring in skin, UPS is difficult to differentiate from atypical fibroxanthoma or dermatofibrosarcoma protuberans (see this term). Histological differential diagnoses include leiomyosarcoma, rhabdomyosarcoma, lymphoma, and melanoma (see these terms). Management and treatment UPS should be referred to an expert/ reference center for primary biopsy, expert pathology review, and multidisciplinary treatment. Immediate surgery of a mass without knowledge of its histological nature is strongly discouraged because it is associated with an increased risk of death due to inappropriate resection and increased risk of relapse. UPS is best treated by wide surgical excision. Sometimes amputation may be necessary to remove the whole lesion. Adjuvant radiotherapy is given for high-grade, large (>5 cm), deep-seated tumors, in limb sparing surgeries and when negative margins are not obtained. For non-operable sarcomas, primary radiation therapy could be an option, but usually doxorubicin containing regimens are preferred options in first-line setting for locally irresectable and/or metastatic lesions. Chemotherapy (CHT) with ifosfamide, trabectedin, dacarbazine, pazopanib have demonstrated efficacy in UPS and are registered and available in most European Union countries. Prognosis A 5-year overall survival rate of 48% has been reported for patients with head and neck tumors versus 77% for patients with tumors arising on the trunk and extremities. The childhood variant appears have better prognosis. Visit the Orphanet disease page for more resources.

MalaCards based summary : Undifferentiated Pleomorphic Sarcoma, also known as malignant fibrous histiocytoma, is related to malignant skin fibrous histiocytoma and ovarian clear cell carcinoma. An important gene associated with Undifferentiated Pleomorphic Sarcoma is RECQL4 (RecQ Like Helicase 4), and among its related pathways/superpathways are HIV Life Cycle and Developmental Biology. The drugs Ifosfamide and Lenograstim have been mentioned in the context of this disorder. Affiliated tissues include bone, lung and breast, and related phenotypes are abnormality of the lower limb and abnormality of the peritoneum

Wikipedia : 74 Undifferentiated pleomorphic sarcoma, previously malignant fibrous histiocytoma, is a type of cancer,... more...

Related Diseases for Undifferentiated Pleomorphic Sarcoma

Diseases related to Undifferentiated Pleomorphic Sarcoma via text searches within MalaCards or GeneCards Suite gene sharing:

(showing 5628, show less)
# Related Disease Score Top Affiliating Genes
1 malignant skin fibrous histiocytoma 32.9 MLANA KIT
2 ovarian clear cell carcinoma 31.4 PIK3CA MET KRAS
3 anus cancer 31.4 PIK3CA KRAS KIT
4 giant cell glioblastoma 31.4 PDGFRA IDH2 IDH1
5 carney triad 31.0 PDGFRA KIT
6 oligodendroglioma 30.9 PDGFRA NTRK1 IDH2 IDH1
7 retroperitoneal sarcoma 30.9 MLANA KIT
8 enchondroma 30.8 IDH2 IDH1
9 neurilemmoma 30.7 PDGFRA KIT EZR
10 chordoma 30.7 PDGFRA MET IDH1
11 leiomyosarcoma 30.6 PDGFRA MLANA KIT
12 differentiated thyroid carcinoma 30.6 NTRK1 MET KRAS
13 meningioma, familial 30.5 MLANA KIT IDH1 EZR
14 angiosarcoma 30.4 MLANA KRAS KIT
15 neurofibromatosis, type i 30.4 PDGFRA KIT
16 neurofibroma 30.3 PDGFRA MLANA KIT
17 intrahepatic cholangiocarcinoma 30.3 KRAS IDH2 IDH1
18 fibrosarcoma of bone 30.2 PDGFRA KIT
19 sarcoma 30.1 STAT3 PIK3CA PDGFRA MET KRAS KIT
20 hypereosinophilic syndrome 30.1 STAT3 PDGFRA KIT
21 malignant peripheral nerve sheath tumor 30.1 PDGFRA MLANA MET KIT
22 muscle cancer 30.1 PDGFRA MLANA KIT
23 mixed glioma 30.1 PDGFRA IDH2 IDH1
24 large cell carcinoma 30.0 PDGFRA KRAS KIT
25 carcinosarcoma 30.0 PIK3CA KRAS KIT
26 rhabdomyosarcoma 29.9 PDGFRA MET KRAS KIT EZR
27 neurofibromatosis, type iv, of riccardi 29.9 PDGFRA KRAS KIT EZR
28 gastrointestinal stromal tumor 29.9 PDGFRA MIR152 KRAS KIT
29 myeloid leukemia 29.8 STAT3 KRAS KIT IDH2 IDH1
30 cellular myxoid liposarcoma 29.8 PIK3CA KIT
31 gliosarcoma 29.7 PDGFRA IDH2 IDH1
32 cytogenetically normal acute myeloid leukemia 29.7 IDH2 IDH1
33 cerebellar astrocytoma 29.7 IDH2 IDH1
34 pulmonary vein stenosis 29.7 PDGFRA KIT
35 melanoma, uveal 29.7 MLANA MET KIT EZR
36 small cell carcinoma 29.6 PDGFRA KRAS KIT
37 colorectal adenocarcinoma 29.6 STAT3 KRAS KIT
38 adenocarcinoma 29.5 STAT3 PIK3CA MET KRAS KIT
39 myelofibrosis 29.5 STAT3 KIT IDH2 IDH1
40 mastocytosis 29.5 PDGFRA NTRK1 KIT
41 grade iii astrocytoma 29.5 PDGFRA IDH2 IDH1
42 peripheral nervous system neoplasm 29.5 PRDM10 NTRK1 KIT
43 mesenchymal cell neoplasm 29.4 PDGFRA NTRK1 MLANA KIT
44 hypereosinophilic syndrome, idiopathic 29.4 PDGFRA KIT
45 chondroblastic osteosarcoma 29.3 IDH2 IDH1 EZR
46 essential thrombocythemia 29.3 STAT3 KIT IDH2 IDH1
47 glioma 29.3 PIK3CA PDGFRA MET IDH2 IDH1
48 myelodysplastic syndrome 29.3 STAT3 KRAS KIT IDH2 IDH1
49 cervical squamous cell carcinoma 29.3 STAT3 PIK3CA KRAS
50 breast duct papilloma 29.3 IDH2 IDH1
51 clear cell chondrosarcoma 29.2 IDH2 IDH1
52 rosai-dorfman disease 29.2 PDGFRA KRAS
53 core binding factor acute myeloid leukemia 29.2 KRAS KIT
54 li-fraumeni syndrome 29.2 RECQL4 KRAS IDH1
55 systemic mastocytosis 29.2 PDGFRA KIT IDH2 IDH1
56 adenosquamous carcinoma 29.2 PIK3CA KRAS KIT
57 gastric leiomyoma 29.1 PDGFRA KIT
58 gastric leiomyosarcoma 29.1 PDGFRA KIT
59 chronic myelomonocytic leukemia 29.1 PDGFRA KRAS KIT
60 bladder urothelial carcinoma 29.1 PIK3CA PDGFRA KRAS KIT IDH1
61 gemistocytic astrocytoma 29.0 IDH2 IDH1
62 vulvar melanoma 29.0 MLANA KIT
63 leukemia, chronic myeloid 29.0 STAT3 PDGFRA NTRK1 KRAS KIT
64 myeloproliferative neoplasm 28.9 STAT3 PDGFRA KIT IDH1
65 chronic leukemia 28.9 STAT3 PDGFRA KIT
66 polycythemia vera 28.8 STAT3 PDGFRA KIT IDH2 IDH1
67 glioma susceptibility 1 28.8 PIK3CA PDGFRA IDH2 IDH1
68 thyroid gland cancer 28.8 PIK3CA NTRK1 MET KRAS KIT
69 fibrillary astrocytoma 28.7 PDGFRA IDH2 IDH1
70 myeloma, multiple 28.7 STAT3 PRDM10 MET KRAS KIT IDH2
71 melanoma 28.6 PIK3CA PDGFRA MLANA MET KRAS KIT
72 gastric adenocarcinoma 28.6 STAT3 PIK3CA MET KRAS KIT EZR
73 intestinal benign neoplasm 28.6 STAT3 PIK3CA KRAS
74 cholangiocarcinoma 28.4 STAT3 PIK3CA MIR152 MET KRAS IDH2
75 costello syndrome 28.4 PIK3CA PDGFRA KRAS
76 neuroblastoma 28.4 STAT3 PIK3CA NTRK1 MIR152 MET KIT
77 ovary adenocarcinoma 28.3 PRDM10 PIK3CA KRAS
78 endometrial cancer 28.3 STAT3 PIK3CA PDGFRA KRAS KIT EZR
79 pancreatic adenocarcinoma 28.2 STAT3 PIK3CA NTRK1 MET KRAS KIT
80 adenoid cystic carcinoma 28.2 STAT3 PIK3CA NTRK1 KRAS KIT IDH1
81 brain cancer 28.2 STAT3 PIK3CA PDGFRA IDH2 IDH1 EZR
82 glioblastoma multiforme 28.1 STAT3 PIK3CA PDGFRA MET KRAS KIT
83 renal cell carcinoma, papillary, 1 28.1 PIK3CA NTRK1 MET KIT
84 medulloblastoma 28.0 STAT3 PIK3CA PDGFRA NTRK1 MET KIT
85 brain stem glioma 28.0 PIK3CA PDGFRA IDH2 IDH1
86 ovarian disease 27.8 STAT3 PRDM10 PIK3CA KRAS KIT
87 muscular disease 27.7 STAT3 PRDM10 PDGFRA LMNA KIT
88 leukemia, acute myeloid 27.7 STAT3 PRDM10 PDGFRA NTRK1 KRAS KIT
89 suppression of tumorigenicity 12 27.7 STAT3 PRDM10 PIK3CA KRAS KIT IDH1
90 ovarian cancer 27.4 STAT3 PIK3CA PDGFRA NTRK1 MIR152 MET
91 lung cancer susceptibility 3 27.1 STAT3 PRDM10 PIK3CA NTRK1 MET KRAS
92 retinitis pigmentosa 27.0 STAT3 PRDM10 PDGFRA NTRK1 LMNA KIT
93 diaphyseal medullary stenosis with malignant fibrous histiocytoma 13.1
94 malignant fibrous histiocytoma of bone 12.8
95 kabuki syndrome 1 12.2
96 malignant fibroxanthoma 11.9
97 histiocytoma, angiomatoid fibrous 11.8
98 porphyria, acute intermittent 11.8
99 mastocytosis, cutaneous 11.5
100 frontotemporal lobar degeneration with tdp43 inclusions, grn-related 11.5
101 urachal cancer 11.5
102 migraine with or without aura 1 11.4
103 vascular disease 11.3
104 peripheral vascular disease 11.3
105 atherosclerosis susceptibility 11.3
106 amyloidosis, hereditary, transthyretin-related 11.3
107 eating disorder 11.3
108 nephrolithiasis, calcium oxalate 11.3
109 narcolepsy 11.3
110 coronary heart disease 1 11.3
111 carpal tunnel syndrome 11.3
112 muscular dystrophy, duchenne type 11.2
113 psoriasis 11.2
114 wilson disease 11.2
115 oral and digital anomalies with ichthyosis 11.2
116 esophageal cancer 11.2
117 cystic fibrosis 11.2
118 refractive error 11.2
119 citrullinemia, classic 11.2
120 lysosomal acid lipase deficiency 11.2
121 sleep disorder 11.2
122 hernia, hiatus 11.2
123 lung cancer 11.2
124 crohn's disease 11.2
125 angina pectoris 11.2
126 bipolar disorder 11.2
127 spinal cord injury 11.2
128 lipid metabolism disorder 11.2
129 systemic lupus erythematosus 11.2
130 chronic kidney disease 11.2
131 hyperthyroidism 11.2
132 dementia, lewy body 11.2
133 metachromatic leukodystrophy 11.1
134 diabetes mellitus, permanent neonatal 11.1
135 alzheimer disease 11.1
136 transient cerebral ischemia 11.1
137 endometriosis 11.1
138 fatty liver disease 11.1
139 otitis media 11.1
140 delayed sleep phase disorder 11.1
141 congenital hypopituitarism 11.1
142 obsessive-compulsive disorder 11.1
143 dermatitis, atopic 11.1
144 episodic kinesigenic dyskinesia 1 11.1
145 glaucoma-related pigment dispersion syndrome 11.1
146 rippling muscle disease 2 11.1
147 spinal cord disease 11.1
148 dementia 11.1
149 bronchitis 11.1
150 poliomyelitis 11.1
151 amyloidosis 11.1
152 spondyloarthropathy 1 11.1
153 non-alcoholic fatty liver disease 11.1
154 cleft lip/palate 11.1
155 pure autonomic failure 11.1
156 diabetes mellitus, noninsulin-dependent 11.1
157 bronchiectasis 11.1
158 phenylketonuria 11.1
159 peripheral artery disease 11.1
160 herpes zoster 11.1
161 diabetes mellitus, insulin-dependent 11.1
162 acute promyelocytic leukemia 11.1
163 fabry disease 11.1
164 gaucher disease, type i 11.1
165 congenital toxoplasmosis 11.1
166 porphyria 11.1
167 chronic thromboembolic pulmonary hypertension 11.1
168 al amyloidosis 11.1
169 carotid artery disease 11.1
170 hypogonadotropic hypogonadism 11.1
171 stevens-johnson syndrome/toxic epidermal necrolysis 11.1
172 lymphangioleiomyomatosis 11.1
173 cystic kidney disease 11.1
174 cluster headache 11.1
175 myopia 11.1
176 niemann-pick disease 11.1
177 autoimmune lymphoproliferative syndrome 11.1
178 cystinosis 11.1
179 muscular dystrophy, congenital, lmna-related 11.1
180 paralytic poliomyelitis 11.1
181 alcoholic liver cirrhosis 11.1
182 neuronal ceroid lipofuscinosis 11.1
183 hyperlipoproteinemia, type iii 11.1
184 common cold 11.1
185 farsightedness 11.1
186 protoporphyria, erythropoietic, 1 11.1
187 dandy-walker syndrome 11.1
188 neurodegeneration with brain iron accumulation 1 11.1
189 tay-sachs disease 11.1
190 lesch-nyhan syndrome 11.1
191 intrahepatic cholestasis of pregnancy 11.1
192 nocardiosis 11.1
193 dermatitis 11.1
194 alagille syndrome 1 11.1
195 parathyroid carcinoma 11.1
196 lymphatic malformation 5 11.1
197 dubin-johnson syndrome 11.1
198 infantile myofibromatosis 11.1
199 mitochondrial disorders 11.1
200 crigler-najjar syndrome, type i 11.1
201 mannosidosis, alpha b, lysosomal 11.1
202 dieulafoy lesion 11.1
203 cerebral cavernous malformation, familial 11.1
204 ciguatera fish poisoning 11.1
205 myelodysplastic syndrome with excess blasts 11.1
206 atrial standstill 1 11.1
207 attention deficit-hyperactivity disorder 11.1
208 autoimmune disease 11.1
209 osteoporosis 11.1
210 campomelic dysplasia 11.1
211 juvenile polyposis syndrome 11.1
212 cholestasis, progressive familial intrahepatic, 1 11.1
213 anemia, congenital dyserythropoietic, type ia 11.1
214 chylomicron retention disease 11.1
215 glycine encephalopathy 11.1
216 lissencephaly 1 11.1
217 zinc deficiency, transient neonatal 11.1
218 pulmonary alveolar proteinosis, acquired 11.1
219 sydenham chorea 11.1
220 primary cutaneous amyloidosis 11.1
221 familial cold autoinflammatory syndrome 11.1
222 cerebral atherosclerosis 11.1
223 congenital dyserythropoietic anemia 11.1
224 hereditary paraganglioma-pheochromocytoma syndromes 11.1
225 congenital pulmonary alveolar proteinosis 11.1
226 cutaneous mastocytoma 11.1
227 hereditary amyloidosis 11.1
228 paroxysmal hemicrania 11.1
229 recurrent hydatidiform mole 11.1
230 glycogen storage disease type 0 11.1
231 hereditary xanthinuria 11.1
232 gastroesophageal reflux 11.0
233 hepatitis c 11.0
234 seizure disorder 11.0
235 macular degeneration, age-related, 1 11.0
236 hypoxia 11.0
237 head injury 11.0
238 spindle cell sarcoma 11.0
239 allergic rhinitis 11.0
240 hypertension, essential 11.0
241 portal hypertension 11.0
242 multiple sclerosis 11.0
243 keratoconus 11.0
244 acute pancreatitis 11.0
245 borderline personality disorder 11.0
246 meningitis 11.0
247 progressive familial heart block, type ia 11.0
248 relapsing-remitting multiple sclerosis 11.0
249 myasthenia gravis 11.0
250 hepatitis a 11.0
251 juvenile rheumatoid arthritis 11.0
252 iron metabolism disease 11.0
253 acromegaly 11.0
254 pneumonia 11.0
255 parkinson disease, late-onset 11.0
256 polycystic ovary syndrome 11.0
257 tetanus 11.0
258 malaria 11.0
259 patent ductus arteriosus 1 11.0
260 arthritis 11.0
261 neurofibromatosis, type ii 11.0
262 learning disability 11.0
263 gallbladder disease 1 11.0
264 chickenpox 11.0
265 primary biliary cirrhosis 11.0
266 esophageal atresia 11.0
267 optic nerve disease 11.0
268 appendicitis 11.0
269 amblyopia 11.0
270 psoriatic arthritis 11.0
271 cystitis 11.0
272 fibromyalgia 11.0
273 precocious puberty 11.0
274 peptic esophagitis 11.0
275 pericarditis 11.0
276 pituitary tumors 11.0
277 iga glomerulonephritis 11.0
278 aplastic anemia 11.0
279 thyroid carcinoma, familial medullary 11.0
280 generalized anxiety disorder 11.0
281 aortic valve disease 2 11.0
282 cholangitis, primary sclerosing 11.0
283 hairy cell leukemia 11.0
284 diabetic neuropathy 11.0
285 west syndrome 11.0
286 anthracosis 11.0
287 varicocele 11.0
288 guillain-barre syndrome 11.0
289 breast disease 11.0
290 vitiligo-associated multiple autoimmune disease susceptibility 1 11.0
291 focal segmental glomerulosclerosis 11.0
292 exstrophy of bladder 11.0
293 brugada syndrome 11.0
294 azoospermia 11.0
295 embryonal carcinoma 11.0
296 plantar fasciitis 11.0
297 glycogen storage disease ii 11.0
298 tuberous sclerosis 1 11.0
299 budd-chiari syndrome 11.0
300 mycobacterium tuberculosis 1 11.0
301 essential tremor 11.0
302 actinic keratosis 11.0
303 retroperitoneal fibrosis 11.0
304 central serous chorioretinopathy 11.0
305 burkitt lymphoma 11.0
306 aceruloplasminemia 11.0
307 brucellosis 11.0
308 ectodermal dysplasia 11.0
309 oncocytoma 11.0
310 leiomyoma, uterine 10.9
311 broken heart syndrome 10.9
312 coronary artery dissection, spontaneous 10.9
313 fetal alcohol syndrome 10.9
314 bone cancer 10.9
315 transverse myelitis 10.9
316 glycogen storage disease 10.9
317 fainting 10.9
318 hydrocephalus, normal-pressure 10.9
319 esophagitis, eosinophilic, 1 10.9
320 postural orthostatic tachycardia syndrome 10.9
321 common variable immunodeficiency 10.9
322 miliary tuberculosis 10.9
323 myopathy, tubular aggregate, 1 10.9
324 testicular microlithiasis 10.9
325 progressive multifocal leukoencephalopathy 10.9
326 neisseria meningitidis infection 10.9
327 supranuclear palsy, progressive, 1 10.9
328 creutzfeldt-jakob disease 10.9
329 alpha-1-antitrypsin deficiency 10.9
330 restrictive cardiomyopathy 10.9
331 lymphomatoid papulosis 10.9
332 myotonia 10.9
333 facioscapulohumeral muscular dystrophy 1 10.9
334 retinoschisis 1, x-linked, juvenile 10.9
335 hepatic veno-occlusive disease 10.9
336 leukodystrophy 10.9
337 thrombotic thrombocytopenic purpura 10.9
338 inclusion body myositis 10.9
339 panuveitis 10.9
340 shigellosis 10.9
341 transient global amnesia 10.9
342 primary hyperoxaluria 10.9
343 fibrodysplasia ossificans progressiva 10.9
344 noonan syndrome 1 10.9
345 mucopolysaccharidosis, type vi 10.9
346 gangliocytoma 10.9
347 merkel cell carcinoma 10.9
348 anthrax disease 10.9
349 amyloidosis aa 10.9
350 anaplastic oligoastrocytoma 10.9
351 coloboma of macula 10.9
352 nasopharyngitis 10.9
353 genital herpes 10.9
354 epilepsy, myoclonic juvenile 10.9
355 mucopolysaccharidosis, type ii 10.9
356 chronic ulcer of skin 10.9
357 congenital myasthenic syndrome 10.9
358 protein c deficiency 10.9
359 ganglioglioma 10.9
360 renal oncocytoma 10.9
361 tyrosinemia 10.9
362 limb-girdle muscular dystrophy 10.9
363 herpes simplex encephalitis 10.9
364 age-related hearing loss 10.9
365 achondroplasia 10.9
366 carcinoid tumors, intestinal 10.9
367 cyclic neutropenia 10.9
368 exfoliation syndrome 10.9
369 pulmonary hemosiderosis 10.9
370 buerger disease 10.9
371 hydrops fetalis, nonimmune 10.9
372 myopathy, congenital 10.9
373 lambert-eaton myasthenic syndrome 10.9
374 lymphoplasmacytic lymphoma 10.9
375 cat-scratch disease 10.9
376 fallopian tube carcinoma 10.9
377 sick building syndrome 10.9
378 heparin-induced thrombocytopenia 10.9
379 chiari malformation type i 10.9
380 cystinosis, nephropathic 10.9
381 propionic acidemia 10.9
382 long-chain 3-hydroxyacyl-coa dehydrogenase deficiency 10.9
383 peripartum cardiomyopathy 10.9
384 splenic marginal zone lymphoma 10.9
385 bladder exstrophy-epispadias-cloacal exstrophy complex 10.9
386 endometritis 10.9
387 fuchs' endothelial dystrophy 10.9
388 intracranial thrombosis 10.9
389 tetrahydrobiopterin deficiency 10.9
390 oligoastrocytoma 10.9
391 sacrococcygeal teratoma 10.9
392 angelman syndrome 10.9
393 cerebral amyloid angiopathy, cst3-related 10.9
394 pick disease of brain 10.9
395 leigh syndrome 10.9
396 dyskeratosis congenita 10.9
397 nail disease 10.9
398 premenstrual tension 10.9
399 fascioliasis 10.9
400 hepatopulmonary syndrome 10.9
401 cerebellar degeneration 10.9
402 hajdu-cheney syndrome 10.9
403 camurati-engelmann disease 10.9
404 nail-patella syndrome 10.9
405 factor vii deficiency 10.9
406 legionnaire disease 10.9
407 encephalocraniocutaneous lipomatosis 10.9
408 vitelliform macular dystrophy 10.9
409 organic acidemia 10.9
410 congenital fiber-type disproportion 10.9
411 giardiasis 10.9
412 tinea pedis 10.9
413 klebsiella pneumonia 10.9
414 liver angiosarcoma 10.9
415 empty sella syndrome 10.9
416 diffuse idiopathic skeletal hyperostosis 10.9
417 brittle diabetes 10.9
418 pineal cyst 10.9
419 triploidy 10.9
420 isolated pierre robin sequence 10.9
421 iga nephropathy 1 10.9
422 pityriasis rubra pilaris 10.9
423 variegate porphyria 10.9
424 corneal endothelial dystrophy 10.9
425 hemochromatosis, neonatal 10.9
426 multiple acyl-coa dehydrogenase deficiency 10.9
427 homocystinuria due to cystathionine beta-synthase deficiency 10.9
428 mckusick-kaufman syndrome 10.9
429 krabbe disease 10.9
430 mucopolysaccharidosis, type vii 10.9
431 miyoshi muscular dystrophy 1 10.9
432 shwachman-diamond syndrome 1 10.9
433 hyperphenylalaninemia, bh4-deficient, c 10.9
434 refsum disease, classic 10.9
435 abdominal obesity-metabolic syndrome 1 10.9
436 x-linked chondrodysplasia punctata 1 10.9
437 cloacal exstrophy 10.9
438 isolated ectopia lentis 10.9
439 rift valley fever 10.9
440 childhood absence epilepsy 10.9
441 whipple disease 10.9
442 macular telangiectasia type 2 10.9
443 orofacial granulomatosis 10.9
444 proliferative verrucous leukoplakia 10.9
445 hydromyelia 10.9
446 frontonasal dysplasia 1 10.9
447 meralgia paraesthetica, familial 10.9
448 nevus, epidermal 10.9
449 currarino syndrome 10.9
450 septooptic dysplasia 10.9
451 central hypoventilation syndrome, congenital 10.9
452 glutaric acidemia i 10.9
453 neurodegeneration with brain iron accumulation 2a 10.9
454 megaloblastic anemia 1 10.9
455 polycystic kidney disease 4 with or without polycystic liver disease 10.9
456 pendred syndrome 10.9
457 pallister-killian syndrome 10.9
458 alpha-thalassemia 10.9
459 osteofibrous dysplasia 10.9
460 niemann-pick disease, type b 10.9
461 multiple enchondromatosis, maffucci type 10.9
462 sitosterolemia 10.9
463 hemochromatosis type 2 10.9
464 chronic progressive external ophthalmoplegia 10.9
465 protein s deficiency 10.9
466 biliary dyskinesia 10.9
467 akinetic mutism 10.9
468 urea cycle disorder 10.9
469 collagenous gastritis 10.9
470 idiopathic hypersomnia 10.9
471 limbic encephalitis with lgi1 antibodies 10.9
472 primary orthostatic hypotension 10.9
473 specific antibody deficiency 10.9
474 sunct headache 10.9
475 vernal keratoconjunctivitis 10.9
476 meningitis and encephalitis 10.9
477 branchiooculofacial syndrome 10.9
478 cat eye syndrome 10.9
479 diabetes insipidus, neurohypophyseal 10.9
480 gastric cancer, hereditary diffuse 10.9
481 fetal hemoglobin quantitative trait locus 1 10.9
482 otodental dysplasia 10.9
483 hyperkalemic periodic paralysis 10.9
484 spastic paraplegia 4, autosomal dominant 10.9
485 otospondylomegaepiphyseal dysplasia, autosomal dominant 10.9
486 muckle-wells syndrome 10.9
487 denys-drash syndrome 10.9
488 camptodactyly with muscular hypoplasia, skeletal dysplasia, and abnormal palmar creases 10.9
489 fructose intolerance, hereditary 10.9
490 glycogen storage disease ib 10.9
491 n-acetylglutamate synthase deficiency 10.9
492 hyperornithinemia-hyperammonemia-homocitrullinuria syndrome 10.9
493 mandibuloacral dysplasia with type a lipodystrophy 10.9
494 nijmegen breakage syndrome 10.9
495 glutathione synthetase deficiency 10.9
496 pyruvate kinase deficiency of red cells 10.9
497 spondylocarpotarsal synostosis syndrome 10.9
498 methylmalonic aciduria and homocystinuria, cblc type 10.9
499 kabuki syndrome 2 10.9
500 glycerol kinase deficiency 10.9
501 mesomelia-synostoses syndrome 10.9
502 congenital cataracts, facial dysmorphism, and neuropathy 10.9
503 becker nevus syndrome 10.9
504 genitopatellar syndrome 10.9
505 colloid cysts of third ventricle 10.9
506 aminoacylase 1 deficiency 10.9
507 pitt-hopkins syndrome 10.9
508 aromatase deficiency 10.9
509 megalencephalic leukoencephalopathy with subcortical cysts 2b, remitting, with or without mental retardation 10.9
510 acatalasemia 10.9
511 lipedema 10.9
512 familial cold autoinflammatory syndrome 3 10.9
513 hereditary sensory neuropathy 10.9
514 gamma heavy chain disease 10.9
515 crest syndrome 10.9
516 3-methylglutaconic aciduria 10.9
517 fruit allergy 10.9
518 autosomal dominant nocturnal frontal lobe epilepsy 10.9
519 esophageal atresia/tracheoesophageal fistula 10.9
520 tethered spinal cord syndrome 10.9
521 cartilage disease 10.9
522 clonorchiasis 10.9
523 ureteral disease 10.9
524 branchiootorenal syndrome 10.9
525 myotonia congenita 10.9
526 breast malignant phyllodes tumor 10.9
527 gm1 gangliosidosis 10.9
528 orofaciodigital syndrome 10.9
529 calciphylaxis 10.9
530 prosopagnosia 10.9
531 malignant triton tumor 10.9
532 skin tag 10.9
533 amino acid metabolic disorder 10.9
534 acid sphingomyelinase deficiency 10.9
535 diabetes mellitus, 6q24-related transient neonatal 10.9
536 polr3-related leukodystrophy 10.9
537 progressive myoclonus epilepsy, lafora type 10.9
538 48,xxyy syndrome 10.9
539 49,xxxxy syndrome 10.9
540 acute flaccid myelitis 10.9
541 bobble-head doll syndrome 10.9
542 chaotic atrial tachycardia 10.9
543 classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency 10.9
544 congenital extrahepatic portosystemic shunt 10.9
545 congenital varicella syndrome 10.9
546 eosinophilic cystitis 10.9
547 familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis 10.9
548 juvenile ossifying fibroma 10.9
549 lymphomatoid granulomatosis 10.9
550 neonatal adrenoleukodystrophy 10.9
551 nodular regenerative hyperplasia 10.9
552 nontuberculous mycobacterial lung disease 10.9
553 propriospinal myoclonus 10.9
554 thrombotic thrombocytopenic purpura, acquired 10.9
555 virus associated hemophagocytic syndrome 10.9
556 stargardt macular degeneration 10.9
557 familial hyperaldosteronism 10.9
558 rigid spine muscular dystrophy 10.9
559 occipital neuralgia 10.9
560 shaken baby syndrome 10.9
561 kowarski syndrome 10.8
562 ichthyosis, x-linked 10.8
563 spermatogenic failure 16 10.8
564 myostatin-related muscle hypertrophy 10.8
565 histiocytoma 10.8
566 fibrous histiocytoma 10.8
567 anemia, congenital dyserythropoietic, type iii 10.7
568 corneal dystrophy, lattice type i 10.7
569 melanocytic nevus syndrome, congenital 10.7
570 kleine-levin hibernation syndrome 10.7
571 nystagmus, voluntary 10.7
572 buschke-ollendorff syndrome 10.7
573 perry syndrome 10.7
574 premature chromatid separation trait 10.7
575 tarsal-carpal coalition syndrome 10.7
576 3-hydroxyisobutyryl-coa hydrolase deficiency 10.7
577 mayer-rokitansky-kuster-hauser syndrome 10.7
578 barth syndrome 10.7
579 microphthalmia, syndromic 1 10.7
580 trimethylaminuria 10.7
581 hemangioma, capillary infantile 10.7
582 histiocytosis-lymphadenopathy plus syndrome 10.7
583 mitochondrial dna depletion syndrome 5 10.7
584 parkinsonism-dystonia, infantile, 1 10.7
585 immunodeficiency 18 10.7
586 immunodeficiency 19 10.7
587 brown syndrome 10.7
588 hyper-ige recurrent infection syndrome 3, autosomal recessive 10.7
589 carbohydrate metabolic disorder 10.7
590 eosinophilic gastritis 10.7
591 infantile-onset ascending hereditary spastic paralysis 10.7
592 kaposiform lymphangiomatosis 10.7
593 soft tissue sarcoma 10.7
594 renal cell carcinoma, nonpapillary 10.6
595 giant cell tumor 10.6
596 antiphospholipid syndrome, familial 10.6
597 coloboma, ocular, autosomal dominant 10.6
598 darier-white disease 10.6
599 dermatosis papulosa nigra 10.6
600 vibratory urticaria 10.6
601 developmental dysplasia of the hip 1 10.6
602 hyperchlorhidrosis, isolated 10.6
603 nail disorder, nonsyndromic congenital, 2 10.6
604 myopathy, distal, 1 10.6
605 short stature and advanced bone age, with or without early-onset osteoarthritis and/or osteochondritis dissecans 10.6
606 pigmented purpuric eruption 10.6
607 thyrotoxic periodic paralysis 1 10.6
608 trichodentoosseous syndrome 10.6
609 vertical talus, congenital 10.6
610 vertigo, benign recurrent 10.6
611 achondrogenesis, type ii 10.6
612 ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia 10.6
613 atransferrinemia 10.6
614 behr syndrome 10.6
615 calcification of joints and arteries 10.6
616 congenital disorder of glycosylation, type ia 10.6
617 spinocerebellar ataxia, autosomal recessive 2 10.6
618 boucher-neuhauser syndrome 10.6
619 craniodiaphyseal dysplasia 10.6
620 cystinosis, adult nonnephropathic 10.6
621 dihydropyrimidinase deficiency 10.6
622 anemia, congenital dyserythropoietic, type ii 10.6
623 farber lipogranulomatosis 10.6
624 galactokinase deficiency 10.6
625 glycogen storage disease iv 10.6
626 holoprosencephaly 1 10.6
627 urofacial syndrome 1 10.6
628 hyper-beta-alaninemia 10.6
629 hyperphosphatasia with mental retardation syndrome 1 10.6
630 ciliary dyskinesia, primary, 1 10.6
631 succinyl-coa:3-oxoacid-coa transferase deficiency 10.6
632 manitoba oculotrichoanal syndrome 10.6
633 3-methylglutaconic aciduria, type i 10.6
634 mucopolysaccharidosis, type iva 10.6
635 mucopolysaccharidosis, type ivb 10.6
636 spinal muscular atrophy, type iii 10.6
637 secretory component deficiency 10.6
638 sulfite oxidase deficiency, isolated 10.6
639 dihydropyrimidine dehydrogenase deficiency 10.6
640 mismatch repair cancer syndrome 10.6
641 epileptic encephalopathy, early infantile, 2 10.6
642 masa syndrome 10.6
643 aarskog-scott syndrome 10.6
644 renpenning syndrome 1 10.6
645 norrie disease 10.6
646 ornithine transcarbamylase deficiency, hyperammonemia due to 10.6
647 band heterotopia 10.6
648 cleft palate, cardiac defect, genital anomalies, and ectrodactyly 10.6
649 naxos disease 10.6
650 potocki-shaffer syndrome 10.6
651 agammaglobulinemia 1, autosomal recessive 10.6
652 seizures, benign familial infantile, 1 10.6
653 encephalopathy, ethylmalonic 10.6
654 hemochromatosis, type 3 10.6
655 amegakaryocytic thrombocytopenia, congenital 10.6
656 hemochromatosis, type 4 10.6
657 paraganglioma and gastric stromal sarcoma 10.6
658 thyroid carcinoma, hurthle cell 10.6
659 spondyloenchondrodysplasia with immune dysregulation 10.6
660 ciliary dyskinesia, primary, 3 10.6
661 telomere length, mean leukocyte 10.6
662 syncope, familial vasovagal 10.6
663 encephalopathy, acute, infection-induced 1 10.6
664 telangiectasia, hereditary hemorrhagic, type 4 10.6
665 congenital anomalies of kidney and urinary tract 1 10.6
666 ciliary dyskinesia, primary, 7 10.6
667 ciliary dyskinesia, primary, 9 10.6
668 hearing loss, cisplatin-induced 10.6
669 masp2 deficiency 10.6
670 parasomnia, sleepwalking type 10.6
671 retinal arterial macroaneurysm with supravalvular pulmonic stenosis 10.6
672 efavirenz, poor metabolism of 10.6
673 periodic fever, menstrual cycle-dependent 10.6
674 immunodeficiency 14 10.6
675 hemochromatosis, type 5 10.6
676 microphthalmia, syndromic 12 10.6
677 anemia, congenital dyserythropoietic, type ib 10.6
678 vasculitis, autoinflammation, immunodeficiency, and hematologic defects syndrome 10.6
679 xia-gibbs syndrome 10.6
680 helsmoortel-van der aa syndrome 10.6
681 orofaciodigital syndrome xiv 10.6
682 sideroblastic anemia with b-cell immunodeficiency, periodic fevers, and developmental delay 10.6
683 catel-manzke syndrome 10.6
684 hyperproinsulinemia 10.6
685 microcephaly 17, primary, autosomal recessive 10.6
686 rahman syndrome 10.6
687 leukodystrophy, hypomyelinating, 17 10.6
688 mitochondrial complex v deficiency, nuclear type 5 10.6
689 isolated growth hormone deficiency, type iv 10.6
690 autoimmune atherosclerosis 10.6
691 rocky mountain spotted fever 10.6
692 familial partial lipodystrophy 10.6
693 pontocerebellar hypoplasia 10.6
694 kleefstra syndrome 10.6
695 achondrogenesis 10.6
696 hypochondrogenesis 10.6
697 reducing body myopathy 10.6
698 x-linked chondrodysplasia punctata 2 10.6
699 hypermanganesemia with dystonia 10.6
700 tibial muscular dystrophy 10.6
701 mitochondrial complex iii deficiency 10.6
702 diphyllobothriasis 10.6
703 baritosis 10.6
704 western equine encephalitis 10.6
705 tongue disease 10.6
706 lemierre's syndrome 10.6
707 ocular motility disease 10.6
708 corpus luteum cyst 10.6
709 intracranial arteriosclerosis 10.6
710 hypoglossal nerve disease 10.6
711 familial lipoprotein lipase deficiency 10.6
712 benign neonatal seizures 10.6
713 leopard syndrome 10.6
714 cholesterol ester storage disease 10.6
715 geographic tongue 10.6
716 benign familial neonatal epilepsy 10.6
717 penile disease 10.6
718 ocular cancer 10.6
719 uveal disease 10.6
720 mast-cell sarcoma 10.6
721 hair disease 10.6
722 lymphatic system disease 10.6
723 fasciolopsiasis 10.6
724 omsk hemorrhagic fever 10.6
725 isodicentric 15 10.6
726 morquio syndrome 10.6
727 autosomal dominant leukodystrophy with autonomic disease 10.6
728 autosomal dominant tubulointerstitial kidney disease, umod-related 10.6
729 epidermolysis bullosa with pyloric atresia 10.6
730 giant axonal neuropathy 10.6
731 kcnq2-related disorders 10.6
732 mitochondrial membrane protein-associated neurodegeneration 10.6
733 phosphorylase kinase deficiency 10.6
734 8p inverted duplication/deletion syndrome 10.6
735 aquagenic syringeal acrokeratoderma 10.6
736 autosomal dominant deafness-onychodystrophy syndrome 10.6
737 autosomal dominant intellectual disability 49 10.6
738 bamforth syndrome 10.6
739 bullous dystrophy hereditary macular type 10.6
740 chromosome 8p23.1 deletion 10.6
741 distomatosis 10.6
742 episodic angioedema with eosinophilia 10.6
743 erythema nodosum, idiopathic 10.6
744 familial thoracic aortic aneurysm and dissection 10.6
745 fibro-adipose vascular anomaly 10.6
746 hashimoto-pritzker syndrome 10.6
747 his bundle tachycardia 10.6
748 horizontal gaze palsy with progressive scoliosis 10.6
749 klebsiella infection 10.6
750 methylmalonyl-coenzyme a mutase deficiency 10.6
751 myxozoa 10.6
752 necrobiotic xanthogranuloma 10.6
753 non 24 hour sleep wake disorder 10.6
754 pepck 1 deficiency 10.6
755 postorgasmic illness syndrome 10.6
756 recessive dystrophic epidermolysis bullosa-generalized other 10.6
757 sandifer syndrome 10.6
758 scn2a related disorders 10.6
759 sphingosine phosphate lyase insufficiency syndrome 10.6
760 staphylococcal toxic shock syndrome 10.6
761 temporal epilepsy, familial 10.6
762 trigeminal trophic syndrome 10.6
763 trisomy 2 mosaicism 10.6
764 trochleitis 10.6
765 unilateral absence of a pulmonary artery 10.6
766 vitamin b12-responsive methylmalonic acidemia 10.6
767 wolffian tumor 10.6
768 x-linked cerebral adrenoleukodystrophy 10.6
769 x-linked intellectual disability, najm type 10.6
770 cav3-related distal myopathy 10.6
771 autoimmune addison disease 10.6
772 dyserythropoietic anemia and thrombocytopenia 10.6
773 frontotemporal dementia with parkinsonism-17 10.6
774 lattice corneal dystrophy type ii 10.6
775 chronic orthostatic intolerance 10.6
776 deep brain stimulation for movement disorders 10.6
777 mini stroke 10.6
778 multiple system atrophy with orthostatic hypotension 10.6
779 neurological manifestations of pompe disease 10.6
780 neuronal migration disorders 10.6
781 rheumatic encephalitis 10.6
782 syringohydromyelia 10.6
783 congenital erosive and vesicular dermatosis 10.6
784 dermatofibrosarcoma protuberans 10.6
785 inflammatory mfh 10.6
786 myxofibrosarcoma 10.5
787 osteomyelitis 10.5
788 osteoarthritis 10.5
789 mucinous lung adenocarcinoma 10.5 KRAS CD74
790 mammary paget's disease 10.5
791 malignant mesenchymoma 10.5
792 colorectal cancer 10.5
793 sarcoma, synovial 10.4
794 meningioma, radiation-induced 10.4
795 spinal meningioma 10.4
796 spindle cell carcinoma 10.4
797 secretory meningioma 10.4
798 lymphoplasmacyte-rich meningioma 10.4
799 back pain 10.4
800 intracranial chondrosarcoma 10.4 IDH2 IDH1
801 adult brain stem glioma 10.4 IDH2 IDH1
802 central nervous system rhabdomyosarcoma 10.4 IDH2 IDH1
803 periosteal chondrosarcoma 10.4 IDH2 IDH1
804 rare tumor 10.4
805 myxoid liposarcoma 10.4
806 fibrous dysplasia 10.4
807 malignant histiocytosis 10.4
808 47,xyy 10.4
809 scoliosis 10.4
810 breast hemangioma 10.4 IDH2 IDH1
811 juxtacortical chondroma 10.4 IDH2 IDH1
812 dedifferentiated liposarcoma 10.4
813 liposarcoma 10.4
814 adult oligodendroglioma 10.4 IDH2 IDH1
815 neutrophilia, hereditary 10.4
816 histiocytosis 10.4
817 48,xyyy 10.4
818 hypothyroidism 10.4
819 depression 10.4
820 body mass index quantitative trait locus 1 10.4
821 hair whorl 10.3
822 childhood oligodendroglioma 10.3 IDH2 IDH1
823 breast cancer 10.3
824 nasopharyngeal carcinoma 10.3
825 gastrointestinal ulceration, recurrent, with dysfunctional platelets 10.3
826 osteonecrosis 10.3
827 hydronephrosis 10.3
828 transitional cell carcinoma 10.3
829 cutaneous fibrous histiocytoma 10.3
830 bilateral retinoblastoma 10.3
831 hypoglycemia 10.3
832 cataract 10.3
833 personality disorder 10.3
834 mental depression 10.3
835 prostate cancer 10.3
836 tall cell variant papillary carcinoma 10.3 NTRK1 MET
837 vagina leiomyosarcoma 10.3 MLANA KIT
838 cerebral palsy 10.3
839 spinal cord oligodendroglioma 10.3 IDH2 IDH1
840 intraocular pressure quantitative trait locus 10.3
841 end stage renal failure 10.3
842 cervix uteri carcinoma in situ 10.3
843 cervical intraepithelial neoplasia 10.3
844 malignant anus melanoma 10.3 MLANA KIT
845 coronary artery anomaly 10.3
846 interval angle-closure glaucoma 10.3 IDH2 IDH1
847 anxiety 10.3
848 heart disease 10.3
849 uterine corpus sarcoma 10.3 NTRK1 KIT
850 lymphoma, hodgkin, classic 10.3
851 multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia, and hydranencephaly 10.3
852 lymphocytic leukemia 10.3
853 hemangioma 10.3
854 pleomorphic liposarcoma 10.3
855 epithelioid sarcoma 10.3
856 pseudosarcomatous fibromatosis 10.3
857 dysphagia 10.3
858 major affective disorder 8 10.3
859 major affective disorder 9 10.3
860 jejunal neoplasm 10.3 MLANA KIT
861 periodontitis 10.3
862 arteries, anomalies of 10.3
863 malignant dermis tumor 10.3 MLANA KIT
864 major depressive disorder 10.3
865 microvascular complications of diabetes 5 10.3
866 ataxia, combined cerebellar and peripheral, with hearing loss and diabetes mellitus 10.3
867 liver disease 10.3
868 gastritis 10.3
869 prostatic hypertrophy 10.3
870 rectum cancer 10.3
871 chondrosarcoma 10.3
872 neuropathy 10.3
873 atrial fibrillation 10.3
874 inflammatory bowel disease 10.3
875 hepatitis b 10.3
876 traumatic brain injury 10.3
877 sleep apnea 10.3
878 pancreatic cancer 10.3
879 intermediate coronary syndrome 10.3
880 diarrhea 10.2
881 brain injury 10.2
882 bone resorption disease 10.2
883 prostatic adenoma 10.2
884 prostatic hyperplasia, benign 10.2
885 reticular perineurioma 10.2 PDGFRA KIT
886 gliofibroma 10.2 KIT IDH1
887 ovarian clear cell adenofibroma 10.2 PIK3CA KRAS
888 substance abuse 10.2
889 bile duct adenocarcinoma 10.2 KRAS IDH2 IDH1
890 acute cystitis 10.2
891 ventricular septal defect 10.2
892 bone mineral density quantitative trait locus 8 10.2
893 bone mineral density quantitative trait locus 15 10.2
894 rhinitis 10.2
895 deep leiomyoma 10.2 PDGFRA KIT
896 hypercholesterolemia, familial, 1 10.2
897 autism 10.2
898 retinal detachment 10.2
899 infertility 10.2
900 hepatocellular carcinoma 10.2
901 myositis 10.2
902 rhabdoid tumor predisposition syndrome 1 10.2
903 aphasia 10.2
904 lymphoma 10.2
905 mitral valve stenosis 10.2
906 basal cell carcinoma 10.2
907 cystic teratoma 10.2
908 malignant giant cell tumor 10.2
909 lung sarcoma 10.2
910 pleomorphic rhabdomyosarcoma 10.2
911 extraosseous osteosarcoma 10.2
912 rhabdoid cancer 10.2
913 heart valve disease 10.2
914 bone giant cell tumor 10.2
915 extraosseous chondrosarcoma 10.2
916 paraplegia 10.2
917 severe combined immunodeficiency 10.2
918 adenoma 10.2
919 myositis ossificans 10.2
920 sickle cell disease 10.2
921 headache 10.2
922 paraneoplastic syndromes 10.2
923 rare cardiac tumor 10.2
924 histiocytic sarcoma 10.2
925 vasculitis 10.2
926 heart leiomyosarcoma 10.2 PDGFRA KIT
927 astigmatism 10.2
928 idiopathic scoliosis 10.2
929 hydrocephalus 10.2
930 rare adenocarcinoma of the breast 10.2 PIK3CA KRAS
931 colitis 10.2
932 visual epilepsy 10.2
933 thymus clear cell carcinoma 10.2 MLANA KIT
934 anorexia nervosa 10.2
935 cardiac conduction defect 10.2
936 spondylolisthesis 10.2
937 leptin deficiency or dysfunction 10.2
938 open-angle glaucoma 10.2
939 eccrine papillary adenoma 10.2 PIK3CA KRAS
940 atrioventricular block 10.2
941 glomerulonephritis 10.2
942 aortic valve insufficiency 10.2
943 vagina sarcoma 10.2 MLANA KIT
944 sarcoidosis 1 10.2
945 yemenite deaf-blind hypopigmentation syndrome 10.2
946 pustulosis of palm and sole 10.2
947 hyperparathyroidism 10.2
948 cerebellum cancer 10.2 IDH2 IDH1
949 ventricular fibrillation, paroxysmal familial, 1 10.2
950 graft-versus-host disease 10.2
951 dilated cardiomyopathy 10.2
952 mood disorder 10.2
953 osteogenic sarcoma 10.2
954 embryonal sarcoma 10.2
955 pulmonary disease, chronic obstructive 10.2
956 uveitis 10.2
957 small cell cancer of the lung 10.2
958 impotence 10.2
959 tremor 10.2
960 human immunodeficiency virus type 1 10.2
961 psychotic disorder 10.2
962 gestational diabetes 10.2
963 tetralogy of fallot 10.2
964 endometrial small cell carcinoma 10.2 PDGFRA KIT
965 esophagitis 10.2
966 sm-ahnmd 10.2 PDGFRA KIT
967 b-cell lymphoma 10.2
968 goiter 10.2
969 myeloid and lymphoid neoplasms associated with pdgfra rearrangement 10.2 PDGFRA KIT
970 cholangitis 10.2
971 syphilis 10.2
972 encephalopathy 10.2
973 inflammatory spondylopathy 10.1
974 spondylitis 10.1
975 hansen's disease 10.1
976 macular retinal edema 10.1
977 measles 10.1
978 celiac disease 1 10.1
979 leprosy 3 10.1
980 ige responsiveness, atopic 10.1
981 pre-eclampsia 10.1
982 spinal stenosis 10.1
983 muscular dystrophy 10.1
984 synovitis 10.1
985 adenosquamous lung carcinoma 10.1 PIK3CA KRAS
986 arteriovenous malformation 10.1
987 arthropathy 10.1
988 cleft lip 10.1
989 degenerative disc disease 10.1
990 nephrotic syndrome 10.1
991 bladder cancer 10.1
992 kaposi sarcoma 10.1
993 leukemia, chronic lymphocytic 10.1
994 lipomatosis, multiple 10.1
995 pheochromocytoma 10.1
996 suppressor of tumorigenicity 3 10.1
997 hemangiopericytoma, malignant 10.1
998 ocular motor apraxia 10.1
999 reticulum cell sarcoma 10.1
1000 xeroderma pigmentosum, variant type 10.1
1001 ataxia and polyneuropathy, adult-onset 10.1
1002 lymphoma, non-hodgkin, familial 10.1
1003 aneurysmal bone cysts 10.1
1004 chondrosarcoma, extraskeletal myxoid 10.1
1005 gastric cancer 10.1
1006 anaplastic large cell lymphoma 10.1
1007 fibroma 10.1
1008 adrenal gland pheochromocytoma 10.1
1009 inflammatory myofibroblastic tumor 10.1
1010 cardiac arrest 10.1
1011 thrombosis 10.1
1012 pleomorphic lipoma 10.1
1013 pyelonephritis 10.1
1014 xanthogranulomatous pyelonephritis 10.1
1015 cardiac tamponade 10.1
1016 leukemia 10.1
1017 potter's syndrome 10.1
1018 leiomyoma 10.1
1019 lymphangioma 10.1
1020 benign breast phyllodes tumor 10.1
1021 ossifying fibroma 10.1
1022 vulvar sarcoma 10.1
1023 granular cell tumor 10.1
1024 chondroma 10.1
1025 benign mesothelioma 10.1
1026 dermoid cyst 10.1
1027 myoepithelioma 10.1
1028 laryngeal squamous cell carcinoma 10.1
1029 cervix carcinoma 10.1
1030 pulmonary tuberculosis 10.1
1031 acute kidney failure 10.1
1032 cystadenocarcinoma 10.1
1033 ischemia 10.1
1034 teratoma 10.1
1035 plexopathy 10.1
1036 chromophobe adenoma 10.1
1037 radiculopathy 10.1
1038 sebaceous adenocarcinoma 10.1
1039 liver cirrhosis 10.1
1040 inflammatory leiomyosarcoma 10.1
1041 paget's disease of bone 10.1
1042 mature teratoma 10.1
1043 kidney disease 10.1
1044 myxoid chondrosarcoma 10.1
1045 combined t cell and b cell immunodeficiency 10.1
1046 meningothelial meningioma 10.1
1047 diverticulitis 10.1
1048 mediastinitis 10.1
1049 peritonitis 10.1
1050 lung disease 10.1
1051 pulmonary embolism 10.1
1052 chromosomal triplication 10.1
1053 primary bone cancer 10.1
1054 retroperitoneal liposarcoma 10.1
1055 splenomegaly 10.1
1056 aneurysm 10.1
1057 paresthesia 10.1
1058 posttransplant acute limbic encephalitis 10.1
1059 glial tumor 10.1
1060 rapidly involuting congenital hemangioma 10.1
1061 rare lymphatic malformation 10.1
1062 ring chromosome 10.1
1063 rare soft tissue tumor 10.1
1064 pelvic organ prolapse 10.1
1065 avoidant personality disorder 10.1
1066 rare surgical neurologic disease 10.1
1067 pancreatitis 10.1
1068 helicobacter pylori infection 10.1
1069 polyneuropathy 10.1
1070 acute stress disorder 10.1
1071 scoliosis, isolated 1 10.1
1072 skin melanoma 10.1
1073 cytokine deficiency 10.1
1074 autism spectrum disorder 10.1
1075 post-traumatic stress disorder 10.1
1076 hypertrophic cardiomyopathy 10.1
1077 myopathy 10.1
1078 rubella 10.1
1079 gallbladder melanoma 10.1 PDGFRA MLANA
1080 chlamydia 10.1
1081 panic disorder 10.1
1082 schizophrenia 10.1
1083 allergic hypersensitivity disease 10.1
1084 hyperglycemia 10.1
1085 coronary stenosis 10.1
1086 pertussis 10.1
1087 ductal carcinoma in situ 10.1
1088 diabetes mellitus 10.1
1089 myocarditis 10.1
1090 neuritis 10.1
1091 thyroiditis 10.1
1092 scleroderma, familial progressive 10.1
1093 proteasome-associated autoinflammatory syndrome 1 10.1
1094 disease of mental health 10.1
1095 epilepsy 10.1
1096 glomangiomatosis 10.1 MLANA KIT
1097 peripheral nervous system disease 10.1
1098 vesicoureteral reflux 1 10.1
1099 ankylosis 10.1
1100 alpha/beta t-cell lymphopenia with gamma/delta t-cell expansion, severe cytomegalovirus infection, and autoimmunity 10.1
1101 rheumatic disease 10.1
1102 barrett esophagus 10.1
1103 down syndrome 10.1
1104 cholesteatoma of middle ear 10.1
1105 viral hepatitis 10.1
1106 testicular cancer 10.1
1107 purpura 10.1
1108 sensorineural hearing loss 10.1
1109 pik3ca-related overgrowth syndrome 10.1
1110 adult astrocytic tumour 10.1 PDGFRA IDH2 IDH1
1111 chagas disease 10.1
1112 carotid stenosis 10.1
1113 dextro-looped transposition of the great arteries 10.1
1114 amenorrhea 10.1
1115 glaucoma, primary open angle 10.0
1116 hyperinsulinism 10.0
1117 intraductal breast neoplasm 10.0 IDH2 IDH1
1118 alacrima, achalasia, and mental retardation syndrome 10.0
1119 echinococcosis 10.0
1120 asthma 10.0
1121 kawasaki disease 10.0
1122 telangiectasis 10.0
1123 conduct disorder 10.0
1124 ovarian epithelial cancer 10.0
1125 exudative vitreoretinopathy 1 10.0
1126 follicular lymphoma 10.0
1127 sick sinus syndrome 10.0
1128 root resorption 10.0
1129 vascular dementia 10.0
1130 gingival recession 10.0
1131 orthostatic intolerance 10.0
1132 rheumatic fever 10.0
1133 connective tissue disease 10.0
1134 coarctation of aorta 10.0
1135 tendinitis 10.0
1136 cholestasis 10.0
1137 irritable bowel syndrome 10.0
1138 bronchopulmonary dysplasia 10.0
1139 strabismus 10.0
1140 glucose intolerance 10.0
1141 hepatitis 10.0
1142 achalasia 10.0
1143 mechanical strabismus 10.0
1144 acute graft versus host disease 10.0
1145 immune deficiency disease 10.0
1146 oral cancer 10.0
1147 epidermolytic hyperkeratosis 10.0
1148 intussusception 10.0
1149 muir-torre syndrome 10.0
1150 myelopathy, htlv-1-associated 10.0
1151 pulmonary fibrosis, idiopathic 10.0
1152 retinoblastoma 10.0
1153 varicose veins 10.0
1154 thymoma, familial 10.0
1155 stroke, ischemic 10.0
1156 myocardial infarction 10.0
1157 hydrops, lactic acidosis, and sideroblastic anemia 10.0
1158 gastrointestinal carcinoma 10.0
1159 connective tissue benign neoplasm 10.0
1160 desmoid tumor 10.0
1161 microphthalmia 10.0
1162 respiratory failure 10.0
1163 pulmonary edema 10.0
1164 squamous cell carcinoma 10.0
1165 pancreas sarcoma 10.0
1166 cholecystitis 10.0
1167 connective tissue cancer 10.0
1168 liver sarcoma 10.0
1169 idiopathic interstitial pneumonia 10.0
1170 breast sarcoma 10.0
1171 tropical spastic paraparesis 10.0
1172 embryonal rhabdomyosarcoma 10.0
1173 thymoma 10.0
1174 fibrosarcoma 10.0
1175 skin carcinoma 10.0
1176 aortic aneurysm 10.0
1177 skin disease 10.0
1178 pulmonary fibrosis 10.0
1179 lynch syndrome 10.0
1180 familial retinoblastoma 10.0
1181 heart sarcoma 10.0
1182 well-differentiated liposarcoma 10.0
1183 congestive heart failure 10.0
1184 cowden syndrome 10.0
1185 cerebrovascular disease 10.0
1186 exophthalmos 10.0
1187 acute myocardial infarction 10.0
1188 fasciitis 10.0
1189 fibromatosis 10.0
1190 htlv-1 associated myelopathy/tropical spastic paraparesis 10.0
1191 spastic paraparesis 10.0
1192 bone sarcoma 10.0
1193 thyroid carcinoma 10.0
1194 body mass index quantitative trait locus 11 10.0
1195 infective endocarditis 10.0
1196 primary hyperparathyroidism 10.0
1197 acquired immunodeficiency syndrome 10.0
1198 urticaria 10.0
1199 osteochondrosis 10.0
1200 atrophic gastritis 10.0
1201 schistosoma mansoni infection, susceptibility/ 10.0
1202 schistosomiasis 10.0
1203 bronchiolitis 10.0
1204 cerebral artery occlusion 10.0
1205 amyotrophic lateral sclerosis 1 10.0
1206 lateral sclerosis 10.0
1207 pathologic nystagmus 10.0
1208 overgrowth syndrome 10.0
1209 toxoplasmosis 10.0
1210 haemophilus influenzae 10.0
1211 cleft palate, isolated 10.0
1212 pulmonary hypertension, primary, 1 10.0
1213 uterine body mixed cancer 10.0 PIK3CA KRAS KIT
1214 thalassemia 10.0
1215 raynaud phenomenon 10.0
1216 neural tube defects 10.0
1217 pain agnosia 10.0
1218 dental caries 10.0
1219 spondylosis 10.0
1220 human immunodeficiency virus infectious disease 10.0
1221 schizoaffective disorder 10.0
1222 mixed cell type cancer 10.0 PIK3CA KRAS KIT
1223 subacute delirium 10.0
1224 skin benign neoplasm 10.0
1225 kala-azar 1 10.0
1226 sexual disorder 10.0
1227 clubfoot 10.0
1228 leishmaniasis 10.0
1229 body mass index quantitative trait locus 9 10.0
1230 body mass index quantitative trait locus 8 10.0
1231 body mass index quantitative trait locus 4 10.0
1232 body mass index quantitative trait locus 10 10.0
1233 body mass index quantitative trait locus 7 10.0
1234 body mass index quantitative trait locus 12 10.0
1235 body mass index quantitative trait locus 14 10.0
1236 body mass index quantitative trait locus 18 10.0
1237 body mass index quantitative trait locus 19 10.0
1238 body mass index quantitative trait locus 20 10.0
1239 diffuse large b-cell lymphoma 10.0
1240 neuroretinitis 10.0
1241 eclampsia 10.0
1242 temporal lobe epilepsy 10.0
1243 legg-calve-perthes disease 10.0
1244 bulimia nervosa 10.0
1245 oral squamous cell carcinoma 10.0
1246 esophageal varix 10.0
1247 retinitis 10.0
1248 agoraphobia 10.0
1249 obsolete: squamous cell carcinoma of head and neck 10.0
1250 huntington disease 10.0
1251 optic neuritis 10.0
1252 hypopituitarism 10.0
1253 multiple endocrine neoplasia 10.0
1254 aortic aneurysm, familial abdominal, 1 10.0
1255 alcohol dependence 10.0
1256 bladder diverticulum 10.0
1257 fibrosis of extraocular muscles, congenital, 1 10.0
1258 endosteal hyperostosis, autosomal dominant 10.0
1259 melorheostosis, isolated 10.0
1260 neutrophil migration 10.0
1261 paget disease, extramammary 10.0
1262 prader-willi syndrome 10.0
1263 pseudoachondroplasia 10.0
1264 dowling-degos disease 1 10.0
1265 rheumatoid arthritis 10.0
1266 thrombophilia due to thrombin defect 10.0
1267 thyroid cancer, nonmedullary, 1 10.0
1268 triiodothyronine receptor auxiliary protein 10.0
1269 hemochromatosis, type 1 10.0
1270 rothmund-thomson syndrome, type 2 10.0
1271 insulin-like growth factor i 10.0
1272 werner syndrome 10.0
1273 branchiootic syndrome 1 10.0
1274 sickle cell anemia 10.0
1275 cervical cancer 10.0
1276 langerhans cell histiocytosis 10.0
1277 hepatitis c virus 10.0
1278 factor xi deficiency 10.0
1279 microvascular complications of diabetes 3 10.0
1280 microvascular complications of diabetes 4 10.0
1281 microvascular complications of diabetes 6 10.0
1282 microvascular complications of diabetes 7 10.0
1283 leukemia, acute lymphoblastic 10.0
1284 muscle hypertrophy 10.0
1285 hyperprolactinemia 10.0
1286 deficiency anemia 10.0
1287 pulmonary hypertension 10.0
1288 autoimmune pancreatitis 10.0
1289 aspiration pneumonia 10.0
1290 exanthem 10.0
1291 variola major 10.0
1292 paraganglioma 10.0
1293 limb ischemia 10.0
1294 renal fibrosis 10.0
1295 ameloblastoma 10.0
1296 retroperitoneal neuroblastoma 10.0
1297 osteoblastoma 10.0
1298 ptosis 10.0
1299 inguinal hernia 10.0
1300 dental abscess 10.0
1301 myelomeningocele 10.0
1302 lymphoproliferative syndrome 10.0
1303 bone disease 10.0
1304 childhood acute lymphocytic leukemia 10.0
1305 mucositis 10.0
1306 polycystic kidney disease 10.0
1307 castleman disease 10.0
1308 cysticercosis 10.0
1309 dermatomyositis 10.0
1310 endocarditis 10.0
1311 meningoencephalitis 10.0
1312 gastric ulcer 10.0
1313 disseminated intravascular coagulation 10.0
1314 alternating exotropia 10.0
1315 exotropia 10.0
1316 mitral valve insufficiency 10.0
1317 neutropenia 10.0
1318 graves' disease 10.0
1319 acute leukemia 10.0
1320 gout 10.0
1321 pure red-cell aplasia 10.0
1322 tuberous sclerosis 10.0
1323 patent foramen ovale 10.0
1324 mature cataract 10.0
1325 squamous cell papilloma 10.0
1326 toxic shock syndrome 10.0
1327 frozen shoulder 10.0
1328 alcohol use disorder 10.0
1329 thrombocytopenia 10.0
1330 lymphadenitis 10.0
1331 keratosis 10.0
1332 skeletal tuberculosis 10.0
1333 pneumothorax 10.0
1334 heart septal defect 10.0
1335 ichthyosis 10.0
1336 duodenal ulcer 10.0
1337 vascular cancer 10.0
1338 islet cell tumor 10.0
1339 status epilepticus 10.0
1340 atrial heart septal defect 10.0
1341 exostosis 10.0
1342 constipation 10.0
1343 arteriosclerosis 10.0
1344 larynx cancer 10.0
1345 papilloma 10.0
1346 kidney cancer 10.0
1347 cystadenoma 10.0
1348 chondroblastoma 10.0
1349 mesenchymoma 10.0
1350 skin sarcoma 10.0
1351 hemoglobinopathy 10.0
1352 endometrial adenocarcinoma 10.0
1353 bursitis 10.0
1354 anuria 10.0
1355 mucinous adenocarcinoma 10.0
1356 astrocytoma 10.0
1357 cystic lymphangioma 10.0
1358 inverted papilloma 10.0
1359 thymic carcinoma 10.0
1360 neurofibrosarcoma 10.0
1361 mucinous cystadenocarcinoma 10.0
1362 appendix adenocarcinoma 10.0
1363 breast mucinous carcinoma 10.0
1364 intermittent claudication 10.0
1365 pleural empyema 10.0
1366 pituitary adenoma 10.0
1367 thyroid gland papillary carcinoma 10.0
1368 ectomesenchymoma 10.0
1369 tricuspid valve stenosis 10.0
1370 tricuspid valve insufficiency 10.0
1371 myxosarcoma 10.0
1372 systemic scleroderma 10.0
1373 endometrial stromal sarcoma 10.0
1374 melorheostosis 10.0
1375 smooth muscle tumor 10.0
1376 intracranial embolism 10.0
1377 juvenile xanthogranuloma 10.0
1378 seminoma 10.0
1379 histiocytoid hemangioma 10.0
1380 movement disease 10.0
1381 benign ependymoma 10.0
1382 pleomorphic xanthoastrocytoma 10.0
1383 sclerosing hemangioma 10.0
1384 malignant granular cell myoblastoma 10.0
1385 myxoid leiomyosarcoma 10.0
1386 epulis 10.0
1387 dystonia 10.0
1388 cellular ependymoma 10.0
1389 sarcomatoid squamous cell skin carcinoma 10.0
1390 malignant giant cell tumor of soft parts 10.0
1391 pleomorphic carcinoma 10.0
1392 sclerosing liposarcoma 10.0
1393 parasagittal meningioma 10.0
1394 fibrous meningioma 10.0
1395 active peptic ulcer disease 10.0
1396 peptic ulcer disease 10.0
1397 peptic ulcer perforation 10.0
1398 fibrosarcomatous osteosarcoma 10.0
1399 sarcomatosis 10.0
1400 interdigitating dendritic cell sarcoma 10.0
1401 congenital fibrosarcoma 10.0
1402 polycythemia 10.0
1403 intestinal obstruction 10.0
1404 ileus 10.0
1405 mucormycosis 10.0
1406 reticulosarcoma 10.0
1407 ulcerative colitis 10.0
1408 decubitus ulcer 10.0
1409 in situ carcinoma 10.0
1410 smallpox 10.0
1411 lupus erythematosus 10.0
1412 hard palate cancer 10.0
1413 pemphigus 10.0
1414 carotid artery dissection 10.0
1415 encephalitis 10.0
1416 trichinosis 10.0
1417 alopecia 10.0
1418 eosinophilia-myalgia syndrome 10.0
1419 fasting hypoglycemia 10.0
1420 fibrosing mediastinitis 10.0
1421 fournier gangrene 10.0
1422 germ cells tumors 10.0
1423 granulocytopenia 10.0
1424 heart tumor 10.0
1425 hemangioendothelioma 10.0
1426 kikuchi disease 10.0
1427 mounier-kuhn syndrome 10.0
1428 mycetoma 10.0
1429 nephrogenic systemic fibrosis 10.0
1430 opsoclonus-myoclonus syndrome 10.0
1431 papular mucinosis 10.0
1432 polymyositis 10.0
1433 pyogenic granuloma 10.0
1434 testicular seminoma 10.0
1435 abdominal wall defect 10.0
1436 cerebral aneurysms 10.0
1437 chronic pain 10.0
1438 myoclonus 10.0
1439 spasticity 10.0
1440 syncope 10.0
1441 undifferentiated embryonal sarcoma of the liver 10.0
1442 epithelioid hemangioendothelioma 10.0
1443 elastofibroma dorsi 10.0
1444 juvenile nasopharyngeal angiofibroma 10.0
1445 avascular necrosis 10.0
1446 mucinous cystadenocarcinoma of the pancreas 10.0
1447 paraneoplastic pemphigus 10.0
1448 argyria 10.0
1449 discoid lupus erythematosus 10.0
1450 lymphedema 10.0
1451 solitary bone cyst 10.0
1452 cardiogenic shock 10.0
1453 red cell aplasia 10.0
1454 hypertriglyceridemia, familial 10.0
1455 colorectal adenoma 10.0
1456 bacterial infectious disease 10.0
1457 autosomal recessive disease 10.0
1458 food allergy 10.0
1459 macular holes 10.0
1460 ectopic pregnancy 10.0
1461 suppression amblyopia 10.0
1462 hypospadias 10.0
1463 amnestic disorder 10.0
1464 intracranial aneurysm 10.0
1465 sclerosing cholangitis 10.0
1466 graves disease 1 10.0
1467 enthesopathy 10.0
1468 gastroenteritis 10.0
1469 intracranial hypertension 10.0
1470 hemiplegia 10.0
1471 diphtheria 10.0
1472 osteochondritis dissecans 10.0
1473 chronic fatigue syndrome 10.0
1474 bunion 10.0
1475 hypogonadism 10.0
1476 hypogonadotropism 10.0
1477 herpes simplex 10.0
1478 lymphoma, mucosa-associated lymphoid type 10.0
1479 periodontitis, chronic 10.0
1480 progressive familial heart block, type ib 10.0
1481 tendinopathy 10.0
1482 rheumatic heart disease 10.0
1483 mumps 10.0
1484 papillary carcinoma 10.0
1485 cytomegalovirus infection 10.0
1486 small intestine leiomyoma 10.0 PDGFRA MLANA KIT
1487 aspergillosis 9.9
1488 quadriplegia 9.9
1489 right bundle branch block 9.9
1490 eye disease 9.9
1491 conjunctivitis 9.9
1492 hypotonia 9.9
1493 diaphragmatic hernia, congenital 9.9
1494 trigeminal neuralgia 9.9
1495 hemosiderosis 9.9
1496 facial paralysis 9.9
1497 urethral stricture 9.9
1498 ocular hypertension 9.9
1499 chronic graft versus host disease 9.9
1500 enterocolitis 9.9
1501 hutterite cerebroosteonephrodysplasia syndrome 9.9
1502 tardive dyskinesia 9.9
1503 wilms tumor 5 9.9
1504 pulmonary fibrosis and/or bone marrow failure, telomere-related, 2 9.9
1505 pachyonychia congenita 3 9.9
1506 focal epilepsy 9.9
1507 severe acute respiratory syndrome 9.9
1508 muscular atrophy 9.9
1509 autonomic dysfunction 9.9
1510 keratitis, hereditary 9.9
1511 mycosis fungoides 9.9
1512 low compliance bladder 9.9
1513 idiopathic avascular necrosis 9.9
1514 gonadal dysgenesis 9.9
1515 renovascular hypertension 9.9
1516 keratopathy 9.9
1517 postpartum depression 9.9
1518 aging 9.9
1519 familial adenomatous polyposis 9.9
1520 cholelithiasis 9.9
1521 dysthymic disorder 9.9
1522 bacteriuria 9.9
1523 retinal vein occlusion 9.9
1524 interstitial lung disease 9.9
1525 thyroid gland medullary carcinoma 9.9
1526 diabetes insipidus 9.9
1527 congenital hypothyroidism 9.9
1528 social phobia 9.9
1529 moyamoya disease 1 9.9
1530 leukemia, acute lymphoblastic 3 9.9
1531 hemopericardium 9.9
1532 neurogenic bladder 9.9
1533 pulmonary valve insufficiency 9.9
1534 contact dermatitis 9.9
1535 growth hormone deficiency 9.9
1536 leukoplakia 9.9
1537 fatty liver disease, nonalcoholic 1 9.9
1538 arrhythmogenic right ventricular cardiomyopathy 9.9
1539 microinvasive gastric cancer 9.9
1540 pericardial effusion 9.9
1541 endogenous depression 9.9
1542 antiphospholipid syndrome 9.9
1543 hemorrhoid 9.9
1544 acute liver failure 9.9
1545 helix syndrome 9.9
1546 hypoparathyroidism 9.9
1547 iron deficiency anemia 9.9
1548 neurotic disorder 9.9
1549 ovarian cyst 9.9
1550 lichen planus 9.9
1551 myotonic dystrophy 9.9
1552 torticollis 9.9
1553 squamous cell carcinoma, head and neck 9.9
1554 crohn's colitis 9.9
1555 venous insufficiency 9.9
1556 left bundle branch hemiblock 9.9
1557 pancreatic ductal adenocarcinoma 9.9
1558 whiplash 9.9
1559 apnea, obstructive sleep 9.9
1560 methane production 9.9
1561 secondary hyperparathyroidism 9.9
1562 hyperuricemia 9.9
1563 gaucher's disease 9.9
1564 conventional fibrosarcoma 9.9 PDGFRA KIT
1565 familial hypercholesterolemia 9.9
1566 prostatitis 9.9
1567 cholera 9.9
1568 tic disorder 9.9
1569 diabetic macular edema 9.9
1570 slipped capital femoral epiphysis 9.9
1571 rare hereditary hemochromatosis 9.9
1572 congenital heart defects, hamartomas of tongue, and polysyndactyly 9.9
1573 microvascular complications of diabetes 1 9.9
1574 microvascular complications of diabetes 2 9.9
1575 membranous nephropathy 9.9
1576 filariasis 9.9
1577 bilirubin metabolic disorder 9.9
1578 multidrug-resistant tuberculosis 9.9
1579 uremia 9.9
1580 tobacco addiction 9.9
1581 hepatic coma 9.9
1582 lobular neoplasia 9.9
1583 turner syndrome 9.9
1584 choriocarcinoma 9.9
1585 stomatitis 9.9
1586 allergic encephalomyelitis 9.9
1587 mantle cell lymphoma 9.9
1588 malignant glioma 9.9
1589 craniopharyngioma 9.9
1590 endophthalmitis 9.9
1591 aortic valve disease 1 9.9
1592 hydatidiform mole, recurrent, 1 9.9
1593 endometrial hyperplasia 9.9
1594 non-alcoholic steatohepatitis 9.9
1595 monocular esotropia 9.9
1596 hepatic encephalopathy 9.9
1597 dumping syndrome 9.9
1598 autoimmune hepatitis 9.9
1599 esotropia 9.9
1600 febrile seizures 9.9
1601 smoking as a quantitative trait locus 3 9.9
1602 male infertility 9.9
1603 acoustic neuroma 9.9
1604 biliary atresia 9.9
1605 epicondylitis 9.9
1606 neuroma 9.9
1607 gestational trophoblastic neoplasm 9.9
1608 fibromuscular dysplasia 9.9
1609 vitiligo-associated multiple autoimmune disease susceptibility 6 9.9
1610 mucopolysaccharidosis-plus syndrome 9.9
1611 sinoatrial node disease 9.9
1612 pneumoconiosis 9.9
1613 choledocholithiasis 9.9
1614 hashimoto thyroiditis 9.9
1615 spondylosis, cervical 9.9
1616 lyme disease 9.9
1617 hemolytic-uremic syndrome 9.9
1618 neuroendocrine tumor 9.9
1619 colon adenocarcinoma 9.9
1620 visceral leishmaniasis 9.9
1621 microcephaly 9.9
1622 anoxia 9.9
1623 uterine carcinosarcoma 9.8 PIK3CA KRAS KIT
1624 lipoid congenital adrenal hyperplasia 9.8
1625 cutaneous t cell lymphoma 9.8
1626 q fever 9.8
1627 cystic echinococcosis 9.8
1628 histoplasmosis 9.8
1629 angiomyolipoma 9.8
1630 brain edema 9.8
1631 aortic disease 9.8
1632 lymphopenia 9.8
1633 rare disease in surgical orthopedic 9.8
1634 marfan syndrome 9.8
1635 arts syndrome 9.8
1636 pyloric stenosis 9.8
1637 candidiasis 9.8
1638 cardiac arrhythmia 9.8
1639 resting heart rate, variation in 9.8
1640 metabolic acidosis 9.8
1641 locked-in syndrome 9.8
1642 bipolar i disorder 9.8
1643 opiate dependence 9.8
1644 mitral valve disease 9.8
1645 allergic asthma 9.8
1646 pituitary adenoma, prolactin-secreting 9.8
1647 ewing sarcoma 9.8
1648 pollen allergy 9.8
1649 rickets 9.8
1650 kuhnt-junius degeneration 9.8
1651 antisocial personality disorder 9.8
1652 portal vein thrombosis 9.8
1653 aggressive periodontitis 9.8
1654 angioedema 9.8
1655 gingivitis 9.8
1656 demyelinating disease 9.8
1657 myelitis 9.8
1658 thyroid gland disease 9.8
1659 t-cell leukemia 9.8
1660 malignant pleural mesothelioma 9.8
1661 bullous pemphigoid 9.8
1662 perinatal necrotizing enterocolitis 9.8
1663 hemophilia 9.8
1664 tuberculous meningitis 9.8
1665 congenital anomalies of kidney and urinary tract 2 9.8
1666 rheumatic fever-related antigen 9.8
1667 chorea, childhood-onset, with psychomotor retardation 9.8
1668 physical disorder 9.8
1669 choreatic disease 9.8
1670 central retinal vein occlusion 9.8
1671 bronchiolitis obliterans 9.8
1672 clear cell renal cell carcinoma 9.8
1673 influenza 9.8
1674 coronary artery aneurysm 9.8
1675 meniere disease 9.8
1676 temporal arteritis 9.8
1677 3-methylglutaconic aciduria, type iii 9.8
1678 oppositional defiant disorder 9.8
1679 neovascular glaucoma 9.8
1680 proctitis 9.8
1681 neuromuscular disease 9.8
1682 monoclonal gammopathy of uncertain significance 9.8
1683 gastrointestinal system disease 9.8
1684 septic arthritis 9.8
1685 autosomal dominant polycystic kidney disease 9.8
1686 bacterial meningitis 9.8
1687 oral leukoplakia 9.8
1688 oral lichen planus 9.8
1689 papillomatosis, confluent and reticulated 9.8
1690 pelvic inflammatory disease 9.8
1691 obstructive jaundice 9.8
1692 somatization disorder 9.8
1693 myoma 9.8
1694 bruxism 9.8
1695 dyslexia 9.8
1696 ureteral obstruction 9.8
1697 neuromyelitis optica 9.8
1698 multiple endocrine neoplasia, type i 9.8
1699 takayasu arteritis 9.8
1700 hydrocephalus, congenital, 1 9.8
1701 homocysteinemia 9.8
1702 diabetes mellitus, ketosis-prone 9.8
1703 marginal zone b-cell lymphoma 9.8
1704 cervical dystonia 9.8
1705 corneal edema 9.8
1706 synostosis 9.8
1707 craniosynostosis 9.8
1708 sensory peripheral neuropathy 9.8
1709 insulinoma 9.8
1710 urinary tract obstruction 9.8
1711 reactive arthritis 9.8
1712 pulmonary valve stenosis 9.8
1713 cryptorchidism, unilateral or bilateral 9.8
1714 apraxia 9.8
1715 rabies 9.8
1716 post-thrombotic syndrome 9.8
1717 thrombophilia 9.8
1718 hemolytic anemia 9.8
1719 lentigines 9.8
1720 beta-thalassemia 9.8
1721 asbestosis 9.8
1722 autonomic neuropathy 9.8
1723 long qt syndrome 9.8
1724 allergic contact dermatitis 9.8
1725 milk allergy 9.8
1726 hypokalemia 9.8
1727 acute pyelonephritis 9.8
1728 inherited metabolic disorder 9.8
1729 placenta disease 9.8
1730 carotid artery occlusion 9.8
1731 intestinal volvulus 9.8
1732 dermatophytosis 9.8
1733 single ventricular heart 9.8
1734 cerebral atrophy 9.8
1735 asbestos intoxication 9.8
1736 pemphigus vulgaris, familial 9.8
1737 wolff-parkinson-white syndrome 9.8
1738 arterial calcification, generalized, of infancy, 1 9.8
1739 ataxia-telangiectasia 9.8
1740 silicosis 9.8
1741 thrombocytopenia due to platelet alloimmunization 9.8
1742 gallbladder cancer 9.8
1743 tracheal stenosis 9.8
1744 myofibroma 9.8
1745 oropharynx cancer 9.8
1746 iridocyclitis 9.8
1747 hydrocele 9.8
1748 central precocious puberty 9.8
1749 vitreoretinopathy 9.8
1750 precursor t-cell acute lymphoblastic leukemia 9.8
1751 brittle bone disorder 9.8
1752 granulomatosis with polyangiitis 9.8
1753 global developmental delay, absent or hypoplastic corpus callosum, and dysmorphic facies 9.8
1754 osteomalacia 9.8
1755 mastitis 9.8
1756 bullous keratopathy 9.8
1757 pulmonary sarcoidosis 9.8
1758 benign paroxysmal positional nystagmus 9.8
1759 hyperostosis 9.8
1760 agammaglobulinemia 9.8
1761 complex regional pain syndrome 9.8
1762 cellulitis 9.8
1763 subvalvular aortic stenosis 9.8
1764 dentinogenesis imperfecta type 2 9.8
1765 pouchitis 9.8
1766 glomerular disease 9.8
1767 major affective disorder 1 9.8
1768 pneumothorax, primary spontaneous 9.8
1769 von hippel-lindau syndrome 9.8
1770 multinodular goiter 9.8
1771 secondary progressive multiple sclerosis 9.8
1772 alexithymia 9.8
1773 nodal marginal zone lymphoma 9.8
1774 short bowel syndrome 9.8
1775 dental pulp necrosis 9.8
1776 conn's syndrome 9.8
1777 alveolar echinococcosis 9.8
1778 vestibular neuronitis 9.8
1779 nodular goiter 9.8
1780 germ cell cancer 9.8
1781 churg-strauss syndrome 9.8
1782 germinoma 9.8
1783 adenocarcinoma in situ 9.8
1784 aortitis 9.8
1785 rosacea 9.8
1786 anca-associated vasculitis 9.8
1787 osteonecrosis of the jaw 9.8
1788 gilles de la tourette syndrome 9.8
1789 syringomyelia, noncommunicating isolated 9.8
1790 thrombocytopenic purpura, autoimmune 9.8
1791 vitreoretinopathy, neovascular inflammatory 9.8
1792 kearns-sayre syndrome 9.8
1793 ovarian hyperstimulation syndrome 9.8
1794 cyanosis, transient neonatal 9.8
1795 tick-borne encephalitis 9.8
1796 spastic cerebral palsy 9.8
1797 stuttering 9.8
1798 renal hypertension 9.8
1799 migraine without aura 9.8
1800 spondylolysis 9.8
1801 membranoproliferative glomerulonephritis 9.8
1802 central nervous system lymphoma 9.8
1803 syringomyelia 9.8
1804 hypersplenism 9.8
1805 retinal degeneration 9.8
1806 alopecia areata 9.8
1807 drug dependence 9.8
1808 primary central nervous system lymphoma 9.8
1809 virus-associated trichodysplasia spinulosa 9.8
1810 early-onset schizophrenia 9.8
1811 pfeiffer syndrome 9.7
1812 adenomyosis 9.7
1813 pervasive developmental disorder 9.7
1814 sleeping sickness 9.7
1815 spastic diplegia 9.7
1816 hyperandrogenism 9.7
1817 otosclerosis 9.7
1818 posterior uveitis 9.7
1819 megaesophagus 9.7
1820 breast fibroadenoma 9.7
1821 pharyngitis 9.7
1822 chondromalacia 9.7
1823 mixed connective tissue disease 9.7
1824 plasmacytoma 9.7
1825 compartment syndrome 9.7
1826 hepatoblastoma 9.7
1827 scotoma 9.7
1828 polyarteritis nodosa 9.7
1829 keloid disorder 9.7
1830 post-transplant lymphoproliferative disease 9.7
1831 hand skill, relative 9.7
1832 mesothelioma, malignant 9.7
1833 peutz-jeghers syndrome 9.7
1834 intervertebral disc disease 9.7
1835 west nile virus 9.7
1836 speech and communication disorders 9.7
1837 peyronie's disease 9.7
1838 vitamin b12 deficiency 9.7
1839 zollinger-ellison syndrome 9.7
1840 umbilical hernia 9.7
1841 respiratory allergy 9.7
1842 gastric lymphoma 9.7
1843 japanese encephalitis 9.7
1844 trachoma 9.7
1845 spinal muscular atrophy 9.7
1846 pancytopenia 9.7
1847 acute kidney tubular necrosis 9.7
1848 nephrocalcinosis 9.7
1849 periventricular leukomalacia 9.7
1850 bone inflammation disease 9.7
1851 plague 9.7
1852 retinal disease 9.7
1853 dwarfism 9.7
1854 multiple system atrophy 1 9.7
1855 pectus excavatum 9.7
1856 osteoid osteoma 9.7
1857 ossification of the posterior longitudinal ligament of spine 9.7
1858 aortic aneurysm, familial thoracic 1 9.7
1859 alkuraya-kucinskas syndrome 9.7
1860 encephalopathy, progressive, early-onset, with episodic rhabdomyolysis 9.7
1861 chikungunya 9.7
1862 constrictive pericarditis 9.7
1863 onchocerciasis 9.7
1864 hypochondriasis 9.7
1865 shoulder impingement syndrome 9.7
1866 corneal ectasia 9.7
1867 retinal vascular disease 9.7
1868 pleomorphic adenoma 9.7
1869 proliferative glomerulonephritis 9.7
1870 acute disseminated encephalomyelitis 9.7
1871 parathyroid adenoma 9.7
1872 macroglobulinemia 9.7
1873 substance dependence 9.7
1874 hyperphenylalaninemia 9.7
1875 allergic angiitis 9.7
1876 congenital cytomegalovirus 9.7
1877 posterior urethral valves 9.7
1878 congenital amyoplasia 9.7
1879 peyronie disease 9.7
1880 mccune-albright syndrome 9.7
1881 tracheoesophageal fistula with or without esophageal atresia 9.7
1882 arachnoid cysts, intracranial 9.7
1883 sjogren syndrome 9.7
1884 asplenia, isolated congenital 9.7
1885 sudden infant death syndrome 9.7
1886 bile duct cysts 9.7
1887 pulmonary hypertension, chronic thromboembolic, without deep vein thrombosis 9.7
1888 adrenal cortical carcinoma 9.7
1889 chronic venous insufficiency 9.7
1890 pulpitis 9.7
1891 anogenital venereal wart 9.7
1892 pathological gambling 9.7
1893 hypertrophic pyloric stenosis 9.7
1894 epidermolysis bullosa 9.7
1895 acute myocarditis 9.7
1896 chronic inflammatory demyelinating polyradiculoneuropathy 9.7
1897 pituitary gland disease 9.7
1898 keratoconjunctivitis 9.7
1899 pulmonary emphysema 9.7
1900 hypoplastic left heart syndrome 9.7
1901 microscopic polyangiitis 9.7
1902 osteochondroma 9.7
1903 teeth, supernumerary 9.7
1904 hypertension, early-onset, autosomal dominant, with severe exacerbation in pregnancy 9.7
1905 bone mineral density quantitative trait locus 3 9.7
1906 hypophosphatemia 9.7
1907 ileitis 9.7
1908 trypanosomiasis 9.7
1909 tonsillitis 9.7
1910 paracoccidioidomycosis 9.7
1911 cardiovascular system disease 9.7
1912 thoracic outlet syndrome 9.7
1913 lactic acidosis 9.7
1914 thrombophlebitis 9.7
1915 large intestine cancer 9.7
1916 childhood leukemia 9.7
1917 extrinsic allergic alveolitis 9.7
1918 kidney angiomyolipoma 9.7
1919 hypopharynx cancer 9.7
1920 speech disorder 9.7
1921 sudden sensorineural hearing loss 9.7
1922 x-linked intellectual disability-macrocephaly-macroorchidism syndrome 9.7
1923 cell type benign neoplasm 9.7 PIK3CA MLANA KRAS KIT
1924 factor viii deficiency 9.7
1925 hemifacial microsomia 9.7
1926 polykaryocytosis inducer 9.7
1927 williams-beuren syndrome 9.7
1928 adrenocortical carcinoma, hereditary 9.7
1929 respiratory distress syndrome in premature infants 9.7
1930 fragile x syndrome 9.7
1931 hemophilia a 9.7
1932 myocardial infarction 2 9.7
1933 tendinosis 9.7
1934 erythema multiforme 9.7
1935 restless legs syndrome 9.7
1936 spondyloarthropathy 9.7
1937 infant gynecomastia 9.7
1938 filarial elephantiasis 9.7
1939 anisometropia 9.7
1940 gynecomastia 9.7
1941 kwashiorkor 9.7
1942 interstitial cystitis 9.7
1943 papilledema 9.7
1944 dysostosis 9.7
1945 gingival overgrowth 9.7
1946 anovulation 9.7
1947 adrenal cortical adenocarcinoma 9.7
1948 mutism 9.7
1949 tinea capitis 9.7
1950 inferior myocardial infarction 9.7
1951 inflammatory breast carcinoma 9.7
1952 nervous system disease 9.7
1953 chorioretinitis 9.7
1954 cutaneous leishmaniasis 9.7
1955 thyroid tumor 9.7
1956 thyroid cancer, nonmedullary, 2 9.7
1957 adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency 9.7
1958 reflex sympathetic dystrophy 9.7
1959 hearing loss, noise-induced 9.7
1960 spastic paraplegia, intellectual disability, nystagmus, and obesity 9.7
1961 adult t-cell leukemia 9.7
1962 alcohol-related birth defect 9.7
1963 female breast cancer 9.7
1964 dry eye syndrome 9.7
1965 schizotypal personality disorder 9.7
1966 asphyxia neonatorum 9.7
1967 retinal vasculitis 9.7
1968 presbyopia 9.7
1969 gastroparesis 9.7
1970 dysentery 9.7
1971 newborn respiratory distress syndrome 9.7
1972 algoneurodystrophy 9.7
1973 renal tubular acidosis 9.7
1974 thrombocytosis 9.7
1975 pigmented villonodular synovitis 9.7
1976 early myoclonic encephalopathy 9.7
1977 chronic granulomatous disease 9.7
1978 coronary aneurysm 9.7
1979 thyroid gland follicular carcinoma 9.7
1980 polyradiculoneuropathy 9.7
1981 adjustment disorder 9.7
1982 systolic heart failure 9.7
1983 tenosynovitis 9.7
1984 villonodular synovitis 9.7
1985 congenital rubella 9.7
1986 odontoma 9.7
1987 spondylarthropathy 9.7
1988 foot drop 9.7
1989 undetermined colitis 9.7
1990 erythroleukemia, familial 9.7
1991 hemifacial spasm, familial 9.7
1992 papillon-lefevre syndrome 9.7
1993 familial mediterranean fever 9.7
1994 subacute sclerosing panencephalitis 9.7
1995 pituitary hormone deficiency, combined, 2 9.7
1996 late-onset retinal degeneration 9.7
1997 angioid streaks 9.7
1998 invasive aspergillosis 9.7
1999 hyperphosphatemia 9.7
2000 lennox-gastaut syndrome 9.7
2001 gallbladder disease 9.7
2002 spinal disease 9.7
2003 malignant hypertension 9.7
2004 enophthalmos 9.7
2005 choroiditis 9.7
2006 suppurative otitis media 9.7
2007 childhood type dermatomyositis 9.7
2008 hepatitis d 9.7
2009 kernicterus 9.7
2010 bacterial vaginosis 9.7
2011 coronary restenosis 9.7
2012 egg allergy 9.7
2013 adrenomyeloneuropathy 9.7
2014 congenital torticollis 9.7
2015 homologous wasting disease 9.7
2016 nonseminomatous germ cell tumor 9.7
2017 opioid addiction 9.7
2018 hemifacial spasm 9.7
2019 multicystic dysplastic kidney 9.7
2020 cerebrofacial arteriovenous metameric syndrome 9.7
2021 erythema multiforme major 9.7
2022 coxa vara 9.6
2023 lichen sclerosus et atrophicus 9.6
2024 gastroschisis 9.6
2025 maple syrup urine disease 9.6
2026 adrenoleukodystrophy 9.6
2027 frontotemporal dementia 9.6
2028 paragangliomas 3 9.6
2029 severe cutaneous adverse reaction 9.6
2030 hypertrophic scars 9.6
2031 anal fistula 9.6
2032 cytomegalovirus retinitis 9.6
2033 migraine with aura 9.6
2034 asymptomatic neurosyphilis 9.6
2035 chronic pyelonephritis 9.6
2036 lepromatous leprosy 9.6
2037 transsexualism 9.6
2038 discitis 9.6
2039 cholecystolithiasis 9.6
2040 hypertensive heart disease 9.6
2041 cauda equina syndrome 9.6
2042 penile cancer 9.6
2043 protein-energy malnutrition 9.6
2044 hereditary hemorrhagic telangiectasia 9.6
2045 keratoconjunctivitis sicca 9.6
2046 severe pre-eclampsia 9.6
2047 iritis 9.6
2048 farmer's lung 9.6
2049 hereditary angioedema 9.6
2050 maxillary sinusitis 9.6
2051 motor neuron disease 9.6
2052 vaccinia 9.6
2053 mucoepidermoid carcinoma 9.6
2054 intestinal disease 9.6
2055 hodgkin's lymphoma, lymphocytic-histiocytic predominance 9.6
2056 priapism 9.6
2057 primary ciliary dyskinesia 9.6
2058 yellow fever 9.6
2059 neurosyphilis 9.6
2060 trochlear dysplasia 9.6
2061 developmental dyspraxia 9.6
2062 b-cell non-hodgkin lymphoma 9.6
2063 malignant tumor of penis 9.6
2064 acanthosis nigricans 9.6
2065 anorectal anomalies 9.6
2066 hypertelorism 9.6
2067 raynaud disease 9.6
2068 spinal arachnoiditis 9.6
2069 galactorrhea 9.6
2070 pulmonary arteriovenous fistulas 9.6
2071 wiskott-aldrich syndrome 9.6
2072 rett syndrome 9.6
2073 polydactyly 9.6
2074 atrioventricular septal defect 9.6
2075 phobia, specific 9.6
2076 chlamydia pneumonia 9.6
2077 tooth agenesis 9.6
2078 extrapulmonary tuberculosis 9.6
2079 distal arthrogryposis 9.6
2080 chorioamnionitis 9.6
2081 immunoglobulin alpha deficiency 9.6
2082 latex allergy 9.6
2083 anomalous left coronary artery from the pulmonary artery 9.6
2084 protein-losing enteropathy 9.6
2085 schizophreniform disorder 9.6
2086 adult respiratory distress syndrome 9.6
2087 horner's syndrome 9.6
2088 arachnoiditis 9.6
2089 allergic bronchopulmonary aspergillosis 9.6
2090 typhoid fever 9.6
2091 cardiac sarcoidosis 9.6
2092 urethritis 9.6
2093 irregular astigmatism 9.6
2094 rectum adenocarcinoma 9.6
2095 orchitis 9.6
2096 phimosis 9.6
2097 cryoglobulinemia 9.6
2098 lysosomal storage disease 9.6
2099 breast adenocarcinoma 9.6
2100 cervical adenocarcinoma 9.6
2101 avian influenza 9.6
2102 prostate disease 9.6
2103 blepharospasm 9.6
2104 testicular germ cell cancer 9.6
2105 gastrinoma 9.6
2106 double outlet right ventricle 9.6
2107 mitochondrial myopathy 9.6
2108 aphthous stomatitis 9.6
2109 vitreous detachment 9.6
2110 congenital syphilis 9.6
2111 developmental coordination disorder 9.6
2112 bowen's disease 9.6
2113 encephalocele 9.6
2114 erythrokeratoderma ''en cocardes'' 9.6
2115 plagiocephaly 9.6
2116 dysautonomia 9.6
2117 univentricular heart 9.6
2118 recurrent acute pancreatitis 9.6
2119 atrial septal aneurysm 9.6
2120 basal cell nevus syndrome 9.6
2121 cherubism 9.6
2122 pilonidal sinus 9.6
2123 cystinuria 9.6
2124 fibrosclerosis, multifocal 9.6
2125 friedreich ataxia 9.6
2126 heart block, congenital 9.6
2127 epilepsy, focal, with speech disorder and with or without mental retardation 9.6
2128 dysphasia, familial developmental 9.6
2129 xanthomatosis 9.6
2130 preterm premature rupture of the membranes 9.6
2131 intestinal schistosomiasis 9.6
2132 peripheral t-cell lymphoma 9.6
2133 specific language impairment 9.6
2134 drug allergy 9.6
2135 igg4-related disease 9.6
2136 bell's palsy 9.6
2137 crescentic glomerulonephritis 9.6
2138 dental fluorosis 9.6
2139 primary angle-closure glaucoma 9.6
2140 chronic purulent otitis media 9.6
2141 adult-onset still's disease 9.6
2142 patellofemoral pain syndrome 9.6
2143 autosomal dominant cerebellar ataxia 9.6
2144 panniculitis 9.6
2145 calcinosis 9.6
2146 giant cell reparative granuloma 9.6
2147 hidradenitis suppurativa 9.6
2148 hidradenitis 9.6
2149 splenic infarction 9.6
2150 landau-kleffner syndrome 9.6
2151 central nervous system disease 9.6
2152 vaginal discharge 9.6
2153 demyelinating polyneuropathy 9.6
2154 follicular adenoma 9.6
2155 juvenile pilocytic astrocytoma 9.6
2156 localized scleroderma 9.6
2157 tongue cancer 9.6
2158 aneurysm of sinus of valsalva 9.6
2159 cerebrospinal fluid leak 9.6
2160 periodontal ehlers-danlos syndrome 9.6
2161 pustular psoriasis 9.6
2162 syndromic craniosynostosis 9.6
2163 specific language disorder 9.6
2164 idiopathic nephrotic syndrome 9.6
2165 congenital pseudoarthrosis of the tibia 9.6
2166 acute radiation syndrome 9.6
2167 homozygous familial hypercholesterolemia 9.6
2168 uterus leiomyosarcoma 9.6 PDGFRA NTRK1 MLANA KIT
2169 corneal dystrophy, fuchs endothelial, 1 9.6
2170 renal hypodysplasia/aplasia 1 9.6
2171 fanconi anemia, complementation group a 9.6
2172 intracranial hypertension, idiopathic 9.6
2173 pulmonic stenosis 9.6
2174 dermatitis herpetiformis, familial 9.6
2175 huntington disease-like 3 9.6
2176 dengue virus 9.6
2177 encephalopathy, progressive, with or without lipodystrophy 9.6
2178 polymicrogyria with or without vascular-type ehlers-danlos syndrome 9.6
2179 asperger syndrome 9.6
2180 primary progressive multiple sclerosis 9.6
2181 salmonellosis 9.6
2182 pleurisy 9.6
2183 sialadenitis 9.6
2184 siderosis 9.6
2185 meningocele 9.6
2186 anhidrosis 9.6
2187 megacolon 9.6
2188 neonatal diabetes mellitus 9.6
2189 blind hypotensive eye 9.6
2190 coronary thrombosis 9.6
2191 pulmonary alveolar proteinosis 9.6
2192 paranoid schizophrenia 9.6
2193 vertebrobasilar insufficiency 9.6
2194 megaloblastic anemia 9.6
2195 root caries 9.6
2196 cryptosporidiosis 9.6
2197 cheilitis 9.6
2198 endodermal sinus tumor 9.6
2199 heel spur 9.6
2200 superficial basal cell carcinoma 9.6
2201 ebola hemorrhagic fever 9.6
2202 lymphocele 9.6
2203 hepatitis e 9.6
2204 arteriosclerosis obliterans 9.6
2205 hemangioblastoma 9.6
2206 ovarian serous cystadenocarcinoma 9.6
2207 subacute thyroiditis 9.6
2208 polyhydramnios 9.6
2209 dermatitis herpetiformis 9.6
2210 rem sleep behavior disorder 9.6
2211 homocystinuria 9.6
2212 viral infectious dise