MCID: ALL026
MIFTS: 64

Allergic Hypersensitivity Disease

Categories: Immune diseases

Aliases & Classifications for Allergic Hypersensitivity Disease

MalaCards integrated aliases for Allergic Hypersensitivity Disease:

Name: Allergic Hypersensitivity Disease 12 15
Hypersensitivity 12 74 43 71
Allergies 15 62
Allergic Disposition 71
Allergic Condition 71
Allergic Reaction 71
Allergic Disease 12
Allergy 17

Classifications:



External Ids:

Disease Ontology 12 DOID:1205
MeSH 43 D006967
NCIt 49 C3114
SNOMED-CT 67 21957007 91232002
ICD10 32 T78.4 T78.40
UMLS 71 C0020517 C0851444 C1527304 more

Summaries for Allergic Hypersensitivity Disease

PubMed Health : 62 About allergies: Allergies arise if the body's immune system overreacts to foreign substances (allergens) that are usually harmless in most people, such as pollen or certain foods. The symptoms can vary a lot. In some cases they are quite mild, but they can also be a real nuisance and have a considerable impact in everyday life. Severe allergic reactions may be life-threatening. There are various treatment options for allergies. Some things that trigger allergies (allergens) are easy to avoid, whereas others aren't. Common allergens include the following:

MalaCards based summary : Allergic Hypersensitivity Disease, also known as hypersensitivity, is related to hypersensitivity reaction type iv disease and aztreonam allergy, and has symptoms including nausea and vomiting, abdominal pain and pruritus. An important gene associated with Allergic Hypersensitivity Disease is IL5 (Interleukin 5), and among its related pathways/superpathways are Innate Immune System and ERK Signaling. The drugs Ketotifen and Hydrocortisone have been mentioned in the context of this disorder. Affiliated tissues include testes, skin and t cells, and related phenotypes are hematopoietic system and immune system

Disease Ontology : 12 An immune system disease that is an exaggerated immune response to allergens, such as insect venom, dust mites, pollen, pet dander, drugs or some foods.

Wikipedia : 74 Hypersensitivity (also called hypersensitivity reaction or intolerance) refers to undesirable reactions... more...

Related Diseases for Allergic Hypersensitivity Disease

Diseases related to Allergic Hypersensitivity Disease via text searches within MalaCards or GeneCards Suite gene sharing:

(showing 2170, show less)
# Related Disease Score Top Affiliating Genes
1 hypersensitivity reaction type iv disease 34.7 IL4 IL10 IFNG
2 aztreonam allergy 34.6 IL5 IL13
3 amoxicillin allergy 34.6 IL3 IGHE
4 cefuroxime allergy 34.5 IL5 IL13
5 cefaclor allergy 34.4 IL5 IL13
6 orange allergy 34.3 IL5 IL13
7 nut allergy 34.1 IL5 IL4 IL13 IL10 IGHE
8 abacavir allergy 34.1 CCL17 CCL11
9 erythema multiforme 33.2 IL5 IL4 IFNG CCL5 CCL17
10 sarcoidosis 1 33.1 IL9 IL13 IFNG CCL5
11 alopecia areata 33.1 IL4 IL13 IL10 IFNG
12 bronchiolitis obliterans 33.0 IL13 IL10 IFNG
13 esophagitis, eosinophilic, 1 33.0 RNASE3 IL5 IL4 IL3 IL13 EPX
14 bullous pemphigoid 32.9 RNASE3 IL5 IL4 IL13 IGHE FCER2
15 allergic asthma 32.8 RNASE3 IL9 IL5 IL4 IL3 IL13
16 dermatitis, atopic 32.7 RNASE3 IL9 IL5 IL4 IL3 IL13
17 mikulicz disease 32.6 IL5 IL4 IL13 IL10
18 autoimmune disease of endocrine system 32.5 IL4 IL10 IFNG
19 autoimmune disease of central nervous system 32.5 IL4 IL13 IL10 IFNG CCL5
20 immune system disease 32.5 IL5 IL4 IL13 IL10 IFNG CCL5
21 autoimmune disease of gastrointestinal tract 32.5 IL4 IL10 IFNG
22 rhinitis 32.3 TPT1 RNASE3 IL9 IL5 IL4 IL13
23 ige responsiveness, atopic 32.3 RNASE3 IL5 IL4 IL13 IL10 IGHE
24 dermatitis 32.2 RNASE3 IL5 IL4 IL13 IL10 IGHE
25 autoimmune disease of musculoskeletal system 32.2 IL4 IL10 IFNG
26 pollen allergy 32.1 RNASE3 IL5 IL3 IL13 EPX
27 allergic rhinitis 32.1 TPT1 RNASE3 IL9 IL5 IL4 IL13
28 food allergy 32.1 TPT1 RNASE3 IL5 IL4 IL13 IL10
29 urticaria 32.0 TPT1 RNASE3 IL5 IL4 IL13 IGHE
30 conjunctivitis 31.9 RNASE3 IL5 IL4 IL13 IL10 IGHE
31 stevens-johnson syndrome/toxic epidermal necrolysis 31.9 IL5 IL13 IFNG CCR3 CCL5 CCL17
32 allergic conjunctivitis 31.8 RNASE3 IL5 IL4 IL13 IL10 IGHE
33 interstitial lung disease 31.8 IL5 IL4 IL13 IL10 IFNG CCL5
34 idiopathic interstitial pneumonia 31.7 IL4 IL13 IFNG
35 contact dermatitis 31.7 IL5 IL4 IL10 IFNG CCL17
36 drug allergy 31.6 TPT1 IL5 IGHE
37 pulmonary fibrosis, idiopathic 31.6 IL9 IL5 IL4 IL13 IL10 IFNG
38 autoimmune disease 31.6 IL9 IL5 IL4 IL13 IL10 IFNG
39 pneumonia 31.6 IL5 IL4 IL13 IL10 IFNG CCL5
40 leishmaniasis 31.6 IL5 IL4 IL13 IL10 IFNG
41 milk allergy 31.5 RNASE3 IL9 IL5 IL4 IL13 IL10
42 skin disease 31.5 RNASE3 IL5 IL4 IL13 IL10 IFNG
43 cytokine deficiency 31.5 IL9 IL5 IL13
44 proteasome-associated autoinflammatory syndrome 1 31.5 RNASE3 IL5 IL4 IL13 IL10 IFNG
45 bronchitis 31.4 RNASE3 IL9 IL5 IL4 IL13 IL10
46 candidiasis 31.4 IL4 IL10 IFNG
47 esophagitis 31.4 IL5 IL4 IL13 IL10 CCR3 CCL24
48 collagen disease 31.4 IL4 IL13 IL10
49 allergic contact dermatitis 31.4 IL9 IL5 IL4 IL10 IFNG CCL17
50 asthma 31.3 TPT1 RNASE3 IL9 IL5 IL4 IL3
51 egg allergy 31.3 IL5 IL4 IL10 IGHE
52 vernal keratoconjunctivitis 31.3 RNASE3 IL5 IL4 IL13 IGHE CCL5
53 tetanus 31.3 IL9 IL5 IL4 IL13 IL10 IFNG
54 keratoconjunctivitis 31.3 RNASE3 IL5 IL4 IL3 IL13 IFNG
55 diphtheria 31.3 IL5 IL4 IL3 IL13 IFNG
56 papillary conjunctivitis 31.3 IL4 CCL24 CCL11
57 giant papillary conjunctivitis 31.2 RNASE3 IL4 CCL24 CCL11
58 atopic keratoconjunctivitis 31.2 RNASE3 IL5 IL4 IL3 IGHE IFNG
59 mycosis fungoides 31.2 IL5 IFNG CCR3 CCL17
60 cutaneous leishmaniasis 31.2 IL5 IL4 IL13 IL10 IFNG FCER2
61 endocarditis 31.2 IL10 IFNG EPX
62 peritonitis 31.2 IL4 IL10 IFNG CCL5
63 respiratory allergy 31.2 RNASE3 IL9 IL5 IL4 IL3 IL13
64 extrinsic allergic alveolitis 31.2 IL10 IGHE FCER2 CCL5
65 hypereosinophilic syndrome 31.2 RNASE3 IL9 IL5 IL4 IL3 IL13
66 immune deficiency disease 31.2 IL4 IL13 IL10 IFNG CCR3 CCL5
67 beta-lactam allergy 31.2 IL4 IL13 IL10 IGHE
68 otitis media 31.2 RNASE3 IL5 IL4 IL10 IGHE IFNG
69 paracoccidioidomycosis 31.2 IL5 IL4 IL10 IFNG
70 visceral leishmaniasis 31.2 IL4 IL13 IL10 IFNG
71 mastocytosis 31.1 IL9 IL4 IL3 IL13
72 ulcerative colitis 31.1 IL4 IL13 IL10 IFNG CCR3
73 corticosteroid allergy 31.1 IL5 IL4 IFNG
74 toxoplasmosis 31.1 IL5 IL4 IL10 IFNG
75 latex allergy 31.1 RNASE3 IL5 IL4 IL13 IGHE IFNG
76 neuritis 31.1 IL4 IL10 IFNG CCL5
77 arthritis 31.1 IL4 IL13 IL10 IFNG CCL5
78 celiac disease 1 31.1 IL5 IL4 IL13 IL10 IFNG
79 lepromatous leprosy 31.1 IL4 IL10 IFNG CCL17
80 chronic rhinitis 31.1 RNASE3 IL5 IL4 IL13 HRH1 EPX
81 chagas disease 31.1 IL4 IL10 IFNG CCL5
82 rubella 31.1 IL5 IL4 IL10 IFNG
83 common cold 31.1 RNASE3 IL5 IL4 IL13 IL10 CCL5
84 lichen planus 31.1 IL4 IL10 IFNG
85 chronic fatigue syndrome 31.0 IL5 IL4 IL13 IL10 IFNG CCL5
86 tuberculoid leprosy 31.0 IL4 IL10 IFNG
87 bronchiolitis 31.0 RNASE3 IL5 IL4 IL13 IL10 IFNG
88 colitis 31.0 IL4 IL13 IL10 IFNG CCR3
89 hashimoto thyroiditis 31.0 IL5 IL4 IL10 IFNG
90 peanut allergy 31.0 IL9 IL5 IL4 IL13 IL10 IGHE
91 lung disease 31.0 RNASE3 IL9 IL5 IL4 IL13 IL10
92 toxocariasis 31.0 RNASE3 IL5 IGHE
93 chlamydia 31.0 IL4 IL10 IFNG
94 inflammatory bowel disease 31.0 IL9 IL5 IL4 IL3 IL13 IL10
95 hyper ige syndrome 31.0 IL4 IGHE IFNG
96 gastroenteritis 31.0 RNASE3 IL5 IL4 IL3 IL10 IFNG
97 cryptococcosis 31.0 IL4 IL13 IL10 IFNG
98 dermatitis herpetiformis 31.0 IL5 IL4 IL10 CCL11
99 poliomyelitis 31.0 IL4 IL10 IFNG
100 vernal conjunctivitis 30.9 RNASE3 IL4 IGHE IFNG EPX
101 q fever 30.9 IL4 IL10 IFNG CCL5
102 eye disease 30.9 IL5 IL4 IL13 IL10 IFNG CCL5
103 intestinal schistosomiasis 30.9 IL5 IL4 IL13 IL10
104 scabies 30.9 IL5 IL10 CCL11
105 chronic conjunctivitis 30.9 RNASE3 IL5 IL4 IL13 IL10 IGHE
106 radiculopathy 30.9 IL13 IL10 CCL5 CCL11
107 stomatitis 30.9 IL4 IL10 IFNG
108 chronic mucocutaneous candidiasis 30.9 IL5 IL4 IL10 IFNG
109 orofacial granulomatosis 30.9 IL4 IL10 IFNG CCR3 CCL5
110 intrinsic asthma 30.9 RNASE3 IL5 IL4 IL3 IL13 IGHE
111 coccidiosis 30.9 IL4 IL10 IFNG
112 nickel allergic contact dermatitis 30.9 IL5 IL4 IL10 IFNG
113 demyelinating disease 30.9 IL4 IL10 IFNG CCL5
114 ascaris lumbricoides infection 30.9 IL5 IL13 IFNG
115 human immunodeficiency virus infectious disease 30.8 IL4 IL10 IFNG CCR3 CCL5
116 trichinosis 30.8 IL9 IL5 IL4 IL3 IL13 IL10
117 aphthous stomatitis 30.8 IL5 IL4 IL10 IFNG
118 cutaneous t cell lymphoma 30.8 IL5 IL4 IFNG CCL17
119 psoriatic arthritis 30.8 IL4 IL13 IL10 IFNG
120 folliculitis 30.8 IL5 IL4 IFNG CCL5 CCL11
121 pulmonary eosinophilia 30.8 RNASE3 IL5 IL4 IL13 EPX CCR3
122 gastroesophageal reflux 30.8 IL5 IL4 CCR3 CCL11
123 schistosomiasis 30.8 RNASE3 IL9 IL5 IL4 IL13 IL10
124 osteomyelitis 30.8 IL4 IL10 IFNG CCL5
125 filariasis 30.8 IL5 IL10 IGHE IFNG CCL5
126 pulmonary disease, chronic obstructive 30.8 RNASE3 IL9 IL5 IL4 IL13 IL10
127 cellulitis 30.8 RNASE3 IL5 IL10
128 conjunctival disease 30.8 RNASE3 IL5 IL4 IL13 IL10 HRH1
129 paranasal sinus disease 30.8 IL5 IL4 IL13 IL10 IFNG
130 autoimmune gastritis 30.8 IL4 IL10 IFNG
131 cough variant asthma 30.8 RNASE3 IL5 IL4 IGHE
132 eales disease 30.8 IL4 IL10 IFNG
133 cutaneous lupus erythematosus 30.8 IL10 IFNG CCL17
134 churg-strauss syndrome 30.8 RNASE3 IL5 IL3 IL10 CCL17 CCL11
135 angioedema 30.8 IL5 IGHE HRH1
136 mycoplasma pneumoniae pneumonia 30.8 IL4 IL13 IL10 IFNG
137 acute graft versus host disease 30.7 IL4 IL10 IFNG
138 tonsillitis 30.7 IL4 IL10 IFNG
139 ileitis 30.7 IL10 CCR3 CCL5
140 lymphoma, hodgkin, classic 30.7 IL9 IL3 IL13 CCL17
141 vulvovaginitis 30.7 IL10 CCL5 CCL11
142 parasitic helminthiasis infectious disease 30.7 RNASE3 IL9 IL5 IL4 IL13 IL10
143 aspergillosis 30.7 IL5 IL4 IL10 IFNG EPX CCL5
144 onchocerciasis 30.7 RNASE3 IL5 IL4 IL13 IGHE FCER2
145 severe combined immunodeficiency, x-linked 30.7 IL9 IL4 IL13
146 subacute sclerosing panencephalitis 30.7 IL4 IL10 IFNG
147 polyradiculoneuropathy 30.7 IL10 IFNG CCL5
148 allergic bronchopulmonary aspergillosis 30.7 IL5 IL4 IL10 IGHE IFNG EPX
149 common variable immunodeficiency 30.7 IL5 IL4 IL10 IFNG
150 upper respiratory tract disease 30.6 RNASE3 IL5 IL4 IL13 IL10 IFNG
151 meningitis 30.6 IL5 IL4 IL10 IFNG CCL5
152 chronic eosinophilic pneumonia 30.6 RNASE3 IL5 CCL5 CCL11
153 mucocutaneous leishmaniasis 30.6 IL4 IL10 IFNG
154 myelitis 30.6 IL9 IL10 CCL11
155 leprosy 3 30.6 IL5 IL4 IL10 IFNG
156 cow milk allergy 30.6 RNASE3 IL5 IL4 IL10 CSN1S1
157 penicillin allergy 30.6 IL4 IL13 IL10 IGHE IFNG
158 status asthmaticus 30.6 RNASE3 IL5 IL10 CCL5 CCL11
159 chickenpox 30.6 IL4 IL10 IFNG
160 gingivitis 30.6 IL4 IL10 IFNG CCL5
161 malaria 30.6 TPT1 RNASE3 IL9 IL5 IL4 IL3
162 pemphigoid gestationis 30.6 RNASE3 IL5 CCL11
163 uveitis 30.6 IL9 IL4 IL10 IFNG CCL11
164 hand, foot and mouth disease 30.6 IL13 IL10 IFNG
165 filarial elephantiasis 30.6 IL5 IL4 IL13 IL10
166 scleritis 30.6 IL5 IL4 IFNG
167 chronic inflammatory demyelinating polyradiculoneuropathy 30.6 IL10 IFNG CCL5
168 staphylococcal toxic shock syndrome 30.6 IGHE IFNG
169 leptospirosis 30.6 IL4 IL10 IFNG
170 strongyloidiasis 30.6 IL5 IL3 IL13 IGHE IFNG CCL11
171 opportunistic mycosis 30.6 IL5 IL4 IL13 IL10 IFNG
172 arteriosclerosis 30.5 IL4 IL10 IFNG CCL5 CCL11
173 toxic shock syndrome 30.5 IL4 IL10 IFNG
174 combined t cell and b cell immunodeficiency 30.5 IL9 IL4 IL10
175 trichuriasis 30.5 IL9 IL13 IL10
176 eosinophilic gastroenteritis 30.5 RNASE3 IL5 IL4 IL3 EPX CCL11
177 brucellosis 30.5 IL4 IL10 IFNG
178 viral infectious disease 30.5 IL4 IL13 IL10 IFNG CCR3 CCL5
179 graves' disease 30.5 IL4 IL13 IFNG CCL5
180 angioimmunoblastic lymphadenopathy with dysproteinemia 30.5 IL5 IL13
181 hepatitis a 30.5 IL4 IL10 IFNG
182 relapsing-remitting multiple sclerosis 30.5 IL4 IL10 IFNG CCL5
183 human immunodeficiency virus type 1 30.5 IL10 IFNG CCR3 CCL5 CCL11
184 severe combined immunodeficiency 30.5 IL9 IL5 IL4 IL3 IL13 IL10
185 uveal disease 30.5 IL4 IL10 IFNG
186 bronchial disease 30.5 RNASE3 IL9 IL5 IL4 IL13 IL10
187 yellow fever 30.5 IL5 IL4 CCL5
188 severe acute respiratory syndrome 30.5 IL10 IFNG CCL5
189 diabetes mellitus, insulin-dependent 30.5 IL4 IL13 IL10 IFNG CCL11
190 eosinophilic pneumonia 30.5 RNASE3 IL5 IL4 IL3 IL13 CCL5
191 psoriasis 30.5 IL5 IL4 IL13 IL10 IFNG CCL5
192 idiopathic nephrotic syndrome 30.5 IL4 IGHE
193 spondyloarthropathy 30.4 IL4 IL10 IFNG
194 kimura disease 30.4 RNASE3 IL5 IL4 IL13 IGHE CCR3
195 behcet syndrome 30.4 IL4 IL13 IL10 IFNG
196 respiratory failure 30.4 RNASE3 IL5 IL13 IL10 EPX CCL5
197 spotted fever 30.4 IL10 IFNG CCL5
198 chronic graft versus host disease 30.4 IL10 IFNG
199 multiple sclerosis 30.4 IL9 IL5 IL4 IL13 IL10 IFNG
200 clonorchiasis 30.4 IL10 IGHE IFNG
201 persistent polyclonal b-cell lymphocytosis 30.4 IL4 FCER2
202 blepharoconjunctivitis 30.4 RNASE3 IL4 CCL24 CCL11
203 dengue hemorrhagic fever 30.4 IL4 IL13 IL10 IFNG
204 cystic echinococcosis 30.4 IL10 IGHE IFNG
205 plasmodium falciparum malaria 30.4 IL4 IL10 IFNG
206 parasitic protozoa infectious disease 30.4 IL5 IL4 IL13 IL10 IFNG
207 secondary progressive multiple sclerosis 30.4 IL4 IL10 IFNG CCR3
208 ceftriaxone allergy 30.4 IL5 IL13
209 metal allergy 30.4 IL4 IL10
210 omenn syndrome 30.4 IL5 IL4 IL10 IGHE IFNG
211 genital herpes 30.3 IL4 IL10 CCL5
212 autoimmune uveitis 30.3 IL4 IL10 IFNG
213 echinococcosis 30.3 RNASE3 IL5 IL10 IGHE IFNG CCL17
214 eosinophilic meningitis 30.3 IL5 IL4 IL13 IL10 IGHE CCL24
215 eosinophilic gastritis 30.3 IL5 IL13 EPX CCR3 CCL24 CCL11
216 urinary schistosomiasis 30.3 RNASE3 IL5 IL4 IL13 IGHE IFNG
217 pyelonephritis 30.2 IL10 IFNG CCL5
218 stachybotrys chartarum 30.2 IL3 CCL5
219 diclofenac allergy 30.2 IL3 CCR3
220 pulmonary tuberculosis 30.0 IL4 IL10 IFNG
221 periodontitis 29.7 IL4 IL10 IFNG
222 hypersensitivity vasculitis 12.7
223 hypersensitivity pneumonitis, familial 12.6
224 sulfonamide allergy 12.5
225 hypersensitivity reaction type iii disease 12.4
226 lidocaine allergy 12.4
227 isoniazide allergy 12.4
228 succinylcholine allergy 12.4
229 chloramine t respiratory allergy 12.4
230 rocuronium allergy 12.4
231 crab allergy 12.4
232 carbamazepine allergy 12.4
233 mepivacaine allergy 12.4
234 melon allergy 12.4
235 cherry allergy 12.4
236 gluten allergy 12.4
237 chicken egg allergy 12.4
238 crustacean allergy 12.3
239 snail allergy 12.3
240 quinidine allergy 12.3
241 timothy grass allergy 12.3
242 goat milk allergy 12.3
243 co-trimoxazole allergy 12.3
244 trimethoprim allergy 12.3
245 sulfasalazine allergy 12.3
246 thiopental allergy 12.3
247 ceftazidime allergy 12.3
248 insect stings, hypersensitivity to 12.3
249 amodiaquine allergy 12.3
250 melphalan allergy 12.3
251 apricot allergy 12.3
252 ranitidine allergy 12.2
253 suprofen allergy 12.2
254 d-mannitol allergy 12.2
255 cyclophosphamide allergy 12.2
256 tubocurarine allergy 12.2
257 meropenem allergy 12.2
258 remazole black respiratory allergy 12.2
259 4-vinylcyclohexene dioxide respiratory allergy 12.2
260 sodium aurothiomalate allergy 12.2
261 disodium cromoglycate allergy 12.2
262 phthalyl group allergy 12.2
263 indian plum allergy 12.2
264 plum allergy 12.2
265 atlantic cod allergy 12.2
266 atlantic salmon allergy 12.2
267 carp allergy 12.2
268 zebrafish allergy 12.2
269 rainbow trout allergy 12.2
270 brown shrimp allergy 12.2
271 indian prawn allergy 12.2
272 tiger prawn allergy 12.2
273 white shrimp allergy 12.2
274 cefotaxime allergy 12.2
275 cefixime allergy 12.2
276 piperacillin allergy 12.2
277 alcuronium bromide allergy 12.2
278 gallamine allergy 12.2
279 patent blue v allergy 12.2
280 acid anhydride respiratory allergy 12.2
281 cefotiam allergy 12.2
282 asparagus, specific smell hypersensitivity 12.1
283 obsolete: susceptibility to hypersensitivity syndrome due to abacavir treatment 12.1
284 carbapenem allergy 12.1
285 horned turban snail allergy 12.0
286 erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, and hyper-ige 12.0
287 allergic cutaneous vasculitis 11.8
288 familial cold autoinflammatory syndrome 1 11.7
289 severe cutaneous adverse reaction 11.7
290 bird fancier's lung 11.7
291 wheat allergy 11.6
292 familial cold autoinflammatory syndrome 11.6
293 arthus reaction 11.5
294 bagassosis 11.5
295 erythrocytosis, familial, 1 11.5
296 fanconi anemia, complementation group e 11.5
297 drug reaction with eosinophilia and systemic symptoms 11.5
298 idiopathic infantile hypercalcemia 11.4
299 fanconi anemia, complementation group a 11.4
300 croup 11.4
301 urticaria, aquagenic 11.4
302 fanconi anemia, complementation group c 11.4
303 fanconi anemia, complementation group d2 11.4
304 fanconi anemia, complementation group b 11.4
305 fanconi anemia, complementation group d1 11.4
306 fanconi anemia, complementation group n 11.4
307 fanconi anemia, complementation group o 11.4
308 fanconi anemia, complementation group g 11.4
309 goodpasture syndrome 11.3
310 mushroom workers' lung 11.3
311 xeroderma pigmentosum, variant type 11.3
312 pulmonary sarcoidosis 11.3
313 polycythemia vera 11.3
314 postorgasmic illness syndrome 11.3
315 hypoascorbemia 11.3
316 cyclic vomiting syndrome 11.3
317 bruxism 11.3
318 nijmegen breakage syndrome 11.3
319 juvenile myelomonocytic leukemia 11.3
320 thrombocytopenia-absent radius syndrome 11.3
321 monoclonal mast cell activation syndrome 11.3
322 sjogren syndrome 11.3
323 familial mediterranean fever 11.2
324 hypercalcemia, infantile, 1 11.2
325 enhanced s-cone syndrome 11.2
326 xeroderma pigmentosum, complementation group a 11.2
327 xeroderma pigmentosum, complementation group d 11.2
328 cinca syndrome 11.2
329 fanconi anemia, complementation group u 11.2
330 igg4-related disease 11.2
331 vogt-koyanagi-harada disease 11.2
332 antiphospholipid syndrome 11.2
333 photoallergic dermatitis 11.2
334 subacute bacterial endocarditis 11.2
335 gianotti crosti syndrome 11.2
336 heiner syndrome 11.1
337 hyper-ige recurrent infection syndrome 1, autosomal dominant 11.1
338 hereditary alpha tryptasemia syndrome 11.1
339 dock8 immunodeficiency syndrome 11.1
340 pgm3-congenital disorder of glycosylation 11.1
341 erythrocytosis, familial, 2 11.1
342 fanconi anemia, complementation group f 11.1
343 fanconi anemia, complementation group i 11.1
344 fanconi anemia, complementation group j 11.1
345 fanconi anemia, complementation group l 11.1
346 fanconi anemia, complementation group q 11.1
347 jansen-de vries syndrome 11.1
348 n,n'-diphenylthiourea allergic contact dermatitis 11.0
349 n,n'-diethylthiourea allergic contact dermatitis 11.0
350 rare allergic respiratory disease 11.0
351 eosinophil peroxidase deficiency 10.9
352 selective igm deficiency disease 10.9
353 polyposis, skin pigmentation, alopecia, and fingernail changes 10.9
354 immunodeficiency, x-linked, with magnesium defect, epstein-barr virus infection, and neoplasia 10.9
355 loeys-dietz syndrome 1 10.9
356 alcohol sensitivity, acute 10.9
357 familial cold autoinflammatory syndrome 3 10.9
358 intellectual developmental disorder with speech delay, dysmorphic facies, and t-cell abnormalities 10.9
359 immunodeficiency 58 10.9
360 meningocele 10.9
361 acute contagious conjunctivitis 10.9
362 vulvar disease 10.9
363 48,xxyy syndrome 10.9
364 autosomal dominant intellectual disability 30 10.9
365 pemphigus vulgaris, familial 10.9
366 xeroderma pigmentosum, complementation group c 10.9
367 xeroderma pigmentosum, complementation group e 10.9
368 xeroderma pigmentosum, complementation group f 10.9
369 xeroderma pigmentosum, complementation group g 10.9
370 immunodysregulation, polyendocrinopathy, and enteropathy, x-linked 10.9
371 autoimmune lymphoproliferative syndrome 10.9
372 ataxia-telangiectasia-like disorder 1 10.9
373 xeroderma pigmentosum, complementation group b 10.9
374 warsaw breakage syndrome 10.9
375 tuberculin skin test reactivity, absence of 10.9
376 tuberculin skin test reactivity quantitative trait locus 10.9
377 fanconi anemia, complementation group p 10.9
378 fanconi anemia, complementation group t 10.9
379 fanconi anemia, complementation group v 10.9
380 fanconi anemia, complementation group r 10.9
381 fanconi anemia, complementation group w 10.9
382 fanconi anemia, complementation group s 10.9
383 autoimmune disease of exocrine system 10.9
384 autoimmune disease of eyes, ear, nose and throat 10.9
385 autoimmune disease of skin and connective tissue 10.9
386 autoimmune disease of urogenital tract 10.9
387 autoimmune disease of blood 10.9
388 autoimmune disease of cardiovascular system 10.9
389 heavy chain disease 10.9
390 sting-associated vasculopathy with onset in infancy 10.9
391 paranoid personality disorder 10.9
392 phlyctenulosis 10.9
393 sympathetic ophthalmia 10.9
394 atypical depressive disorder 10.9
395 jaccoud's syndrome 10.9
396 neurosarcoidosis 10.9
397 uveoparotid fever 10.9
398 cardiac sarcoidosis 10.9
399 dipetalonemiasis 10.9
400 cryoglobulinemia 10.9
401 toxicodendron dermatitis 10.9
402 schnitzler syndrome 10.9
403 chronic nk-cell lymphocytosis 10.9
404 loiasis 10.8 IL5 IL4 IL13 IL10
405 respiratory syncytial virus infectious disease 10.8 IL5 IL13 CCL5
406 tropical endomyocardial fibrosis 10.8 IL4 IL10
407 loeffler endocarditis 10.8 RNASE3 IL5 IL3
408 spotted fever rickettsiosis 10.8 IL10 IFNG CCL5
409 b-cell growth factor 10.8 IL4 IL3 IFNG
410 eosinophilic fasciitis 10.8 IL5 IFNG
411 splenic disease 10.8 IL4 IL13 IL10 IFNG
412 primary systemic mycosis 10.8 IL4 IL10 IFNG
413 toxic oil syndrome 10.8 IL5 IL4 IGHE IFNG FCER2
414 african tick-bite fever 10.8 IL13 IL10 IFNG CCL5
415 elephantiasis 10.8 RNASE3 IL5 IL4 IL10 CSN1S1
416 multicentric castleman disease 10.8 IL5 IL10 IFNG
417 idiopathic neutropenia 10.8 IL10 FCER2 CCL5
418 posterior uveitis 10.8 IL9 IL5 IL4 IL13 IFNG
419 paragonimiasis 10.8 RNASE3 IL5 IL13 IGHE CCL17
420 angiostrongyliasis 10.8 IL5 IL4 IL13 CCL24 CCL11
421 endomyocardial fibrosis 10.8 RNASE3 IL5 IL4 IL10 EPX
422 mycetoma 10.8 TPT1 IL10 CSN1S1 CCL5
423 castleman disease 10.8 IL9 IL5 IL4 IL10 IFNG
424 sezary's disease 10.8 IL5 IL4 IL10 IFNG CCL17
425 lymph node disease 10.8 IL4 IL10 IFNG
426 trypanosomiasis 10.8 IL4 IL10 IFNG CCL5
427 leukocyte disease 10.8 IL5 IL4 IL13 IL10
428 primary bacterial infectious disease 10.8 IL5 IL4 IL13 IL10 IFNG CCL5
429 disseminated eosinophilic collagen disease 10.8 RNASE3 IL5 IL3 EPX CCL17
430 commensal bacterial infectious disease 10.7 IL4 IL10 IFNG
431 palladium allergic contact dermatitis 10.7 IL10 CCL17
432 tropical spastic paraparesis 10.7 IL10 IFNG CCL5
433 inflammatory bowel disease 4 10.7 RNASE3 EPX
434 loeffler syndrome 10.7 IL5 IL13
435 testicular disease 10.7 IL4 IL10 IFNG
436 jak3-deficient severe combined immunodeficiency 10.7 IL9 IL4
437 norwegian scabies 10.7 IL5 IL13
438 lymphatic system disease 10.7 IL4 IL10 IFNG
439 autoimmune hepatitis type 1 10.7 IL4 IL10
440 serous labyrinthitis 10.6 CCR3 CCL11
441 adhesive otitis media 10.6 RNASE3 CCL11
442 hypereosinophilic syndrome, idiopathic 10.6 IL5 IL3
443 ventilation pneumonitis 10.6
444 malt worker's lung 10.6
445 cork-handlers' disease 10.6
446 combined thymoma 10.5 IL13 IL10
447 asthma-related traits 4 10.5
448 nose disease 10.5 RNASE3 IL9 IL5 IL4 IL3 IL13
449 nasal cavity disease 10.5 RNASE3 IL9 IL5 IL4 IL3 IL13
450 pulmonary fibrosis 10.5
451 x-linked intellectual disability-macrocephaly-macroorchidism syndrome 10.5
452 erythema multiforme major 10.5
453 chronic pain 10.5
454 neuropathy 10.4
455 gingival recession 10.4
456 house allergic alveolitis 10.3
457 ataxia and polyneuropathy, adult-onset 10.3
458 lymphocytic leukemia 10.3
459 telangiectasis 10.3
460 ataxia-telangiectasia 10.3
461 peripheral nervous system disease 10.3
462 interstitial nephritis 10.3
463 ovarian cancer 10.3
464 leukemia, acute lymphoblastic 10.3
465 herpes simplex 10.3
466 neurodermatitis 10.3
467 nonspecific interstitial pneumonia 10.3
468 alpha/beta t-cell lymphopenia with gamma/delta t-cell expansion, severe cytomegalovirus infection, and autoimmunity 10.2
469 kala-azar 1 10.2
470 spinal cord injury 10.2
471 acute kidney failure 10.2
472 ischemia 10.2
473 vaccinia 10.2
474 bronchiectasis 10.2
475 maple bark strippers' lung 10.2
476 fibrosis of extraocular muscles, congenital, 1 10.2
477 cystic fibrosis 10.2
478 crohn's disease 10.2
479 alopecia 10.2
480 exanthem 10.2
481 measles 10.2
482 erythroleukemia, familial 10.2
483 neutropenia 10.2
484 autism 10.2
485 fibromyalgia 10.2
486 leukemia 10.2
487 pertussis 10.2
488 kidney disease 10.1
489 exfoliative dermatitis 10.1
490 breast cancer 10.1
491 multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia, and hydranencephaly 10.1
492 meniere disease 10.1
493 cholera 10.1
494 hepatitis 10.1
495 acute generalized exanthematous pustulosis 10.1
496 maxillary sinusitis 10.1
497 deficiency anemia 10.1
498 gout 10.1
499 hyperuricemia 10.1
500 irritant dermatitis 10.1
501 fibrosarcoma 10.1
502 skin carcinoma 10.1
503 panic disorder 10.1
504 dentin sensitivity 10.1
505 whiplash 10.1
506 hair whorl 10.1
507 colorectal cancer 10.1
508 granulocytopenia 10.1
509 thalassemia 10.1
510 hemolytic anemia 10.1
511 rapidly involuting congenital hemangioma 10.1
512 c1 inhibitor deficiency 10.0
513 melanoma 10.0
514 cockayne syndrome 10.0
515 attention deficit-hyperactivity disorder 10.0
516 migraine with or without aura 1 10.0
517 rheumatic disease 10.0
518 enthesopathy 10.0
519 lymphocytic choriomeningitis 10.0
520 rheumatic fever 10.0
521 syphilis 10.0
522 myeloid leukemia 10.0
523 chronic purulent otitis media 10.0
524 bladder cancer 10.0
525 osteogenic sarcoma 10.0
526 atrioventricular block 10.0
527 polyneuropathy 10.0
528 bone cancer 10.0
529 iron metabolism disease 10.0
530 immunoglobulin e concentration, serum 10.0
531 body mass index quantitative trait locus 11 10.0
532 body mass index quantitative trait locus 9 10.0
533 body mass index quantitative trait locus 8 10.0
534 body mass index quantitative trait locus 1 10.0
535 body mass index quantitative trait locus 4 10.0
536 body mass index quantitative trait locus 10 10.0
537 body mass index quantitative trait locus 7 10.0
538 body mass index quantitative trait locus 12 10.0
539 body mass index quantitative trait locus 14 10.0
540 body mass index quantitative trait locus 18 10.0
541 body mass index quantitative trait locus 19 10.0
542 body mass index quantitative trait locus 20 10.0
543 irritable bowel syndrome 10.0
544 tardive dyskinesia 10.0
545 cardiac arrest 10.0
546 cholestasis 10.0
547 myeloproliferative neoplasm 10.0
548 hyperthyroidism 10.0
549 herpes zoster 10.0
550 iridocyclitis 10.0
551 hyperacusis 10.0
552 pure autonomic failure 10.0
553 endophthalmitis 10.0
554 middle ear disease 10.0
555 perinatal necrotizing enterocolitis 10.0
556 leukemia, acute myeloid 10.0
557 hyperlipoproteinemia, type iii 10.0
558 pulmonary hypertension 10.0
559 coronary artery anomaly 10.0
560 guillain-barre syndrome 10.0
561 liver disease 10.0
562 congestive heart failure 10.0
563 acquired immunodeficiency syndrome 10.0
564 polycythemia 10.0
565 encephalopathy 10.0
566 helicobacter pylori infection 10.0
567 immunoglobulin alpha deficiency 10.0
568 cystitis 10.0
569 constipation 10.0
570 purpura 10.0
571 thyroiditis 10.0
572 vasculitis 10.0
573 pectus excavatum 10.0
574 chronic venous insufficiency 10.0
575 beta-thalassemia 10.0
576 retinal dystrophy, iris coloboma, and comedogenic acne syndrome 10.0
577 berylliosis 10.0
578 lactose intolerance 10.0
579 disseminated intravascular coagulation 10.0
580 rabies 10.0
581 mononeuropathy 10.0
582 histoplasmosis 10.0
583 embryonal carcinoma 10.0
584 dermatophytosis 10.0
585 heparin-induced thrombocytopenia 10.0
586 hydroa vacciniforme 10.0
587 back pain 10.0
588 hypertension, essential 9.9
589 leukemia, chronic lymphocytic 9.9
590 arteries, anomalies of 9.9
591 myositis 9.9
592 cyanosis, transient neonatal 9.9
593 glucocorticoid resistance, generalized 9.9
594 angina pectoris 9.9
595 pain agnosia 9.9
596 listeriosis 9.9
597 typhoid fever 9.9
598 sick sinus syndrome 9.9
599 orchitis 9.9
600 newcastle disease 9.9
601 pulmonary embolism 9.9
602 dysphagia 9.9
603 chronic beryllium disease 9.9
604 chronic maxillary sinusitis 9.9
605 somatization disorder 9.9
606 triiodothyronine receptor auxiliary protein 9.9
607 kawasaki disease 9.9
608 mumps 9.9
609 bacterial infectious disease 9.9
610 gastritis 9.9
611 neurofibromatosis, type iv, of riccardi 9.9
612 dowling-degos disease 1 9.9
613 myeloma, multiple 9.9
614 myocardial infarction 9.9
615 autosomal recessive disease 9.9
616 pleurisy 9.9
617 iron deficiency anemia 9.9
618 low compliance bladder 9.9
619 coccidioidomycosis 9.9
620 pericarditis 9.9
621 granulomatous hepatitis 9.9
622 endometriosis 9.9
623 glioblastoma multiforme 9.9
624 anthrax disease 9.9
625 malignant hyperthermia 9.9
626 sickle cell disease 9.9
627 beryllium disease 9.9
628 oral lichen planus 9.9
629 hpa i recognition polymorphism, beta-globin-related 9.9
630 burkitt lymphoma 9.9
631 alzheimer disease 9.9
632 alcohol dependence 9.9
633 neutrophil migration 9.9
634 schizophrenia 9.9
635 trigeminal neuralgia 9.9
636 sickle cell anemia 9.9
637 encephalopathy, progressive, early-onset, with episodic rhabdomyolysis 9.9
638 peripheral vascular disease 9.9
639 sarcoma 9.9
640 erysipelas 9.9
641 primary biliary cirrhosis 9.9
642 pancytopenia 9.9
643 blastomycosis 9.9
644 migraine without aura 9.9
645 personality disorder 9.9
646 essential thrombocythemia 9.9
647 synovitis 9.9
648 astrocytoma 9.9
649 hyperglycemia 9.9
650 spindle cell sarcoma 9.9
651 burning mouth syndrome 9.9
652 uremia 9.9
653 acute myocardial infarction 9.9
654 diabetic neuropathy 9.9
655 muscular dystrophy 9.9
656 tremor 9.9
657 acute liver failure 9.9
658 cardiogenic shock 9.9
659 oral squamous cell carcinoma 9.9
660 sensorineural hearing loss 9.9
661 eating disorder 9.9
662 acute articular rheumatism 9.9
663 neurofibromatosis, type ii 9.9
664 schistosoma mansoni infection, susceptibility/ 9.9
665 mycobacterium tuberculosis 1 9.9
666 diarrhea 9.9
667 interstitial cystitis 9.9
668 pharyngitis 9.9
669 multiple chemical sensitivity 9.9
670 allergic encephalomyelitis 9.9
671 pik3ca-related overgrowth syndrome 9.9
672 overgrowth syndrome 9.9
673 huntington disease 9.8
674 kaposi sarcoma 9.8
675 keratitis, hereditary 9.8
676 atrial standstill 1 9.8
677 retinoblastoma 9.8
678 suppressor of tumorigenicity 3 9.8
679 bloom syndrome 9.8
680 paine syndrome 9.8
681 branchiootic syndrome 1 9.8
682 aplastic anemia 9.8
683 pulmonary fibrosis and/or bone marrow failure, telomere-related, 2 9.8
684 helix syndrome 9.8
685 salmonellosis 9.8
686 pulmonary edema 9.8
687 autonomic neuropathy 9.8
688 protein-energy malnutrition 9.8
689 squamous cell papilloma 9.8
690 mental depression 9.8
691 keratosis 9.8
692 dental caries 9.8
693 papilloma 9.8
694 adenocarcinoma 9.8
695 pyoderma 9.8
696 myopathy 9.8
697 spongiotic dermatitis 9.8
698 familial retinoblastoma 9.8
699 peptic ulcer disease 9.8
700 neuroblastoma 9.8
701 osteoarthritis 9.8
702 trichorhinophalangeal syndrome 9.8
703 autoimmune progesterone dermatitis 9.8
704 microscopic polyangiitis 9.8
705 posttransplant acute limbic encephalitis 9.8
706 dermatitis, atopic, 7 9.8
707 foodborne botulism 9.8
708 esophageal atresia 9.8
709 chronic laryngitis 9.8
710 reye syndrome 9.8
711 auditory system disease 9.8
712 bone inflammation disease 9.8
713 somatoform disorder 9.8
714 diffuse glomerulonephritis 9.8
715 dystonia 9.8
716 compartment syndrome 9.8
717 miliary tuberculosis 9.8
718 herpes simplex encephalitis 9.8
719 anoxia 9.8
720 amyotrophic lateral sclerosis 1 9.8
721 thrombophilia due to thrombin defect 9.8
722 acetylation, slow 9.8
723 thymoma, familial 9.8
724 graves disease 1 9.8
725 muscular dystrophy, duchenne type 9.8
726 dermatitis herpetiformis, familial 9.8
727 lymphoma, non-hodgkin, familial 9.8
728 leukemia, chronic myeloid 9.8
729 major depressive disorder 9.8
730 spastic paraplegia, intellectual disability, nystagmus, and obesity 9.8
731 gastrointestinal ulceration, recurrent, with dysfunctional platelets 9.8
732 lymphoblastic lymphoma 9.8
733 neuroretinitis 9.8
734 rickets 9.8
735 japanese encephalitis 9.8
736 borderline personality disorder 9.8
737 hemopericardium 9.8
738 pericardial effusion 9.8
739 coronary artery vasospasm 9.8
740 aseptic meningitis 9.8
741 acute kidney tubular necrosis 9.8
742 acute cystitis 9.8
743 dermatomycosis 9.8
744 squamous cell carcinoma 9.8
745 epilepsy 9.8
746 cholecystitis 9.8
747 cerebral palsy 9.8
748 drug-induced hepatitis 9.8
749 lateral sclerosis 9.8
750 sensory peripheral neuropathy 9.8
751 thymoma 9.8
752 retinitis 9.8
753 shwartzman phenomenon 9.8
754 systemic scleroderma 9.8
755 b-cell lymphoma 9.8
756 pyoderma gangrenosum 9.8
757 intermediate coronary syndrome 9.8
758 amebiasis 9.8
759 fatty liver disease 9.8
760 hypertrophic cardiomyopathy 9.8
761 anca-associated vasculitis 9.8
762 chronic active epstein-barr virus infection 9.8
763 ovarian epithelial cancer 9.8
764 raynaud phenomenon 9.8
765 head injury 9.8
766 hypoxia 9.8
767 systemic lupus erythematosus 9.8
768 gilles de la tourette syndrome 9.8
769 atherosclerosis susceptibility 9.8
770 spondyloarthropathy 1 9.8
771 pulmonary hemosiderosis 9.8
772 rheumatoid arthritis 9.8
773 neural tube defects 9.8
774 enterocolitis 9.8
775 myasthenia gravis 9.8
776 meningioma, radiation-induced 9.8
777 meningioma, familial 9.8
778 dermatitis, atopic, 8 9.8
779 sleep apnea 9.8
780 oppositional defiant disorder 9.8
781 lymphoma 9.8
782 physical urticaria 9.8
783 adenoid hypertrophy 9.8
784 keratoconus 9.8
785 glucose intolerance 9.8
786 allergic urticaria 9.8
787 spinal meningioma 9.8
788 nephrotic syndrome 9.8
789 inflammatory spondylopathy 9.8
790 hemosiderosis 9.8
791 hypothyroidism 9.8
792 agammaglobulinemia 9.8
793 glomerulonephritis 9.8
794 ascaridiasis 9.8
795 mood disorder 9.8
796 laryngitis 9.8
797 occupational dermatitis 9.8
798 secretory meningioma 9.8
799 lymphoplasmacyte-rich meningioma 9.8
800 liver cirrhosis 9.8
801 sleep disorder 9.8
802 connective tissue disease 9.8
803 spondylitis 9.8
804 anisakiasis 9.8
805 gastrointestinal system disease 9.8
806 myocarditis 9.8
807 influenza 9.8
808 lupus erythematosus 9.8
809 encephalitis 9.8
810 pulmonary emphysema 9.8
811 bacterial conjunctivitis 9.8
812 48,xyyy 9.8
813 glioma 9.8
814 glial tumor 9.8
815 hepatocellular carcinoma 9.8
816 motion sickness 9.8
817 osteoporosis 9.8
818 parkinson disease, late-onset 9.8
819 down syndrome 9.8
820 neuropathy, hereditary sensory and autonomic, type iii 9.8
821 halothane hepatitis 9.8
822 ocular motor apraxia 9.8
823 resting heart rate, variation in 9.8
824 bone mineral density quantitative trait locus 8 9.8
825 bone mineral density quantitative trait locus 15 9.8
826 dengue virus 9.8
827 ataxia, combined cerebellar and peripheral, with hearing loss and diabetes mellitus 9.8
828 cephalosporin allergy 9.8
829 pulmonary aspergilloma 9.8
830 cryptogenic organizing pneumonia 9.8
831 trichosporonosis 9.8
832 hypophosphatemia 9.8
833 mantle cell lymphoma 9.8
834 sinoatrial node disease 9.8
835 atrial fibrillation 9.8
836 osteonecrosis 9.8
837 pneumoconiosis 9.8
838 anthracosis 9.8
839 natural killer cell leukemia 9.8
840 dentin caries 9.8
841 meningoencephalitis 9.8
842 pulpitis 9.8
843 trachoma 9.8
844 adult respiratory distress syndrome 9.8
845 heart disease 9.8
846 polycystic ovary syndrome 9.8
847 goiter 9.8
848 tinea pedis 9.8
849 acute leukemia 9.8
850 crescentic glomerulonephritis 9.8
851 porphyria 9.8
852 iritis 9.8
853 panniculitis 9.8
854 status epilepticus 9.8
855 hypogonadism 9.8
856 hyperinsulinism 9.8
857 tularemia 9.8
858 vaginitis 9.8
859 basal cell carcinoma 9.8
860 complex regional pain syndrome 9.8
861 chronic granulomatous disease 9.8
862 teratocarcinoma 9.8
863 inappropriate adh syndrome 9.8
864 mammary paget's disease 9.8
865 plasmacytoma 9.8
866 arthropathy 9.8
867 demyelinating polyneuropathy 9.8
868 hypogonadotropism 9.8
869 chronic kidney disease 9.8
870 intestinal volvulus 9.8
871 retinal degeneration 9.8
872 nervous system disease 9.8
873 bacterial pneumonia 9.8
874 chorioretinitis 9.8
875 ocular hypertension 9.8
876 exercise-induced anaphylaxis 9.8
877 mast cell activation syndrome 9.8
878 mycobacterium chelonae 9.8
879 ocular toxoplasmosis 9.8
880 autonomic dysfunction 9.8
881 dysautonomia 9.8
882 myoclonus 9.8
883 traumatic brain injury 9.8
884 premature aging 9.8
885 thyroid carcinoma 9.8
886 hyperhidrosis, gustatory 9.7
887 intussusception 9.7
888 lichen sclerosus et atrophicus 9.7
889 strabismus 9.7
890 galactosemia 9.7
891 alveolar soft part sarcoma 9.7
892 chromium allergic contact dermatitis 9.7
893 laryngotracheitis 9.7
894 collagenous colitis 9.7
895 angular cheilitis 9.7
896 cryptococcal meningitis 9.7
897 pelvic inflammatory disease 9.7
898 cholelithiasis 9.7
899 hydronephrosis 9.7
900 dengue disease 9.7
901 intermediate uveitis 9.7
902 kwashiorkor 9.7
903 peptic esophagitis 9.7
904 acute diffuse nephritis 9.7
905 geographic tongue 9.7
906 root resorption 9.7
907 labyrinthitis 9.7
908 kidney cancer 9.7
909 long qt syndrome 9.7
910 palmoplantar keratosis 9.7
911 hypotrichosis 9.7
912 viral encephalitis 9.7
913 inherited metabolic disorder 9.7
914 duodenitis 9.7
915 fascioliasis 9.7
916 hard palate cancer 9.7
917 speech disorder 9.7
918 mechanical strabismus 9.7
919 pathologic nystagmus 9.7
920 hemorrhoid 9.7
921 frontal fibrosing alopecia 9.7
922 leukoplakia 9.7
923 neonatal herpes 9.7
924 primary agammaglobulinemia 9.7
925 prosthetic joint infection 9.7
926 specific antibody deficiency 9.7
927 vulvar vestibulitis syndrome 9.7
928 bunion 9.7
929 pneumococcal meningitis 9.7
930 glaucoma, primary open angle 9.7
931 cardiac conduction defect 9.7
932 basal cell nevus syndrome 9.7
933 neutrophilia, hereditary 9.7
934 nevus anemicus 9.7
935 pheochromocytoma 9.7
936 vasculitis, lymphocytic, nodular 9.7
937 periodontitis, chronic 9.7
938 retinitis pigmentosa 9.7
939 roberts syndrome 9.7
940 insulin-like growth factor i 9.7
941 sudden infant death syndrome 9.7
942 fragile x syndrome 9.7
943 aging 9.7
944 cd4/cd8 t-cell ratio 9.7
945 macular degeneration, age-related, 1 9.7
946 langerhans cell histiocytosis 9.7
947 nasopharyngeal carcinoma 9.7
948 neutrophilic dermatosis, acute febrile 9.7
949 endometrial cancer 9.7
950 acute promyelocytic leukemia 9.7
951 mucopolysaccharidosis-plus syndrome 9.7
952 shrimp allergy 9.7
953 invasive aspergillosis 9.7
954 tick-borne encephalitis 9.7
955 variola major 9.7
956 adrenal gland pheochromocytoma 9.7
957 infective endocarditis 9.7
958 pervasive developmental disorder 9.7
959 alexithymia 9.7
960 fruit allergy 9.7
961 apple allergy 9.7
962 childhood acute lymphocytic leukemia 9.7
963 chronic myelomonocytic leukemia 9.7
964 angioimmunoblastic t-cell lymphoma 9.7
965 byssinosis 9.7
966 protein-losing enteropathy 9.7
967 fanconi syndrome 9.7
968 open-angle glaucoma 9.7
969 ornithosis 9.7
970 mitral valve insufficiency 9.7
971 dysentery 9.7
972 dyscalculia 9.7
973 nephrocalcinosis 9.7
974 carotid stenosis 9.7
975 premature ejaculation 9.7
976 inclusion conjunctivitis 9.7
977 lymphogranuloma venereum 9.7
978 sporotrichosis 9.7
979 prostatitis 9.7
980 pneumothorax 9.7
981 rectum adenocarcinoma 9.7
982 post-traumatic stress disorder 9.7
983 dyskeratosis congenita 9.7
984 hairy cell leukemia 9.7
985 acute pancreatitis 9.7
986 iga glomerulonephritis 9.7
987 teratoma 9.7
988 breast adenocarcinoma 9.7
989 systemic mastocytosis 9.7
990 lactic acidosis 9.7
991 ovary adenocarcinoma 9.7
992 porokeratosis 9.7
993 indolent systemic mastocytosis 9.7
994 mesangial proliferative glomerulonephritis 9.7
995 movement disease 9.7
996 agoraphobia 9.7
997 acute stress disorder 9.7
998 premenstrual tension 9.7
999 diverticulitis 9.7
1000 end stage renal failure 9.7
1001 night blindness 9.7
1002 smallpox 9.7
1003 gas gangrene 9.7
1004 achalasia 9.7
1005 pemphigus 9.7
1006 dyskinesia of esophagus 9.7
1007 pompholyx 9.7
1008 exophthalmos 9.7
1009 diabetes insipidus 9.7
1010 cholangitis 9.7
1011 keloid disorder 9.7
1012 microcephaly 9.7
1013 chromosomal triplication 9.7
1014 dwarfism 9.7
1015 germ cells tumors 9.7
1016 herpes zoster ophthalmicus 9.7
1017 hhv-6 encephalitis 9.7
1018 homologous wasting disease 9.7
1019 limbic encephalitis 9.7
1020 polymyositis 9.7
1021 pustular psoriasis 9.7
1022 tuberculous meningitis 9.7
1023 wallerian degeneration 9.7
1024 aneurysm 9.7
1025 cerebral atrophy 9.7
1026 hereditary neuropathies 9.7
1027 stromal keratitis 9.7
1028 drug-induced vasculitis 9.7
1029 virus-associated trichodysplasia spinulosa 9.7
1030 chronic actinic dermatitis 9.7
1031 cancer-associated retinopathy 9.7
1032 pfeiffer syndrome 9.6
1033 immunoglobulin a deficiency 1 9.6
1034 hand skill, relative 9.6
1035 hypercholesterolemia, familial, 1 9.6
1036 hypertriglyceridemia, familial 9.6
1037 ichthyosis vulgaris 9.6
1038 caffey disease 9.6
1039 mastocytosis, cutaneous 9.6
1040 melkersson-rosenthal syndrome 9.6
1041 obsessive-compulsive disorder 9.6
1042 papillomatosis, confluent and reticulated 9.6
1043 scleroderma, familial progressive 9.6
1044 temporal arteritis 9.6
1045 vitiligo-associated multiple autoimmune disease susceptibility 6 9.6
1046 lung cancer 9.6
1047 pancreatic cancer 9.6
1048 skin/hair/eye pigmentation, variation in, 2 9.6
1049 anemia, nonspherocytic hemolytic, due to g6pd deficiency 9.6
1050 taqi polymorphism 9.6
1051 yemenite deaf-blind hypopigmentation syndrome 9.6
1052 cervical cancer 9.6
1053 orthostatic intolerance 9.6
1054 dermatitis, atopic, 3 9.6
1055 dermatitis, atopic, 4 9.6
1056 dermatitis, atopic, 5 9.6
1057 vitiligo-associated multiple autoimmune disease susceptibility 1 9.6
1058 anxiety 9.6
1059 asthma-related traits 2 9.6
1060 granulomatosis with polyangiitis 9.6
1061 hepatitis c virus 9.6
1062 west nile virus 9.6
1063 major affective disorder 8 9.6
1064 major affective disorder 9 9.6
1065 lung cancer susceptibility 3 9.6
1066 asthma-related traits 8 9.6
1067 ectodermal dysplasia-syndactyly syndrome 2 9.6
1068 myelodysplastic syndrome 9.6
1069 graft-versus-host disease 9.6
1070 membranous nephropathy 9.6
1071 striatal degeneration, autosomal dominant 2 9.6
1072 hydrops, lactic acidosis, and sideroblastic anemia 9.6
1073 fetal akinesia deformation sequence 2 9.6
1074 autoimmune pancreatitis 9.6
1075 adenoiditis 9.6
1076 loeys-dietz syndrome 9.6
1077 paralytic poliomyelitis 9.6
1078 chorioamnionitis 9.6
1079 autism spectrum disorder 9.6
1080 fish allergy 9.6
1081 thrombosis 9.6
1082 corneal disease 9.6
1083 dry eye syndrome 9.6
1084 silicosis 9.6
1085 adrenal cortical hypofunction 9.6
1086 pre-eclampsia 9.6
1087 giardiasis 9.6
1088 thrombotic thrombocytopenic purpura 9.6
1089 fiedler's myocarditis 9.6
1090 herpangina 9.6
1091 lipoid nephrosis 9.6
1092 henoch-schoenlein purpura 9.6
1093 anhidrosis 9.6
1094 cercarial dermatitis 9.6
1095 fissured tongue 9.6
1096 myopia 9.6
1097 visual epilepsy 9.6
1098 von willebrand's disease 9.6
1099 brain cancer 9.6
1100 urethritis 9.6
1101 renal tubular acidosis 9.6
1102 cholinergic urticaria 9.6
1103 farmer's lung 9.6
1104 hereditary angioedema 9.6
1105 disease of mental health 9.6
1106 thrombocytopenia due to platelet alloimmunization 9.6
1107 thrombocytopenia 9.6
1108 lymphadenitis 9.6
1109 ichthyosis 9.6
1110 duodenal ulcer 9.6
1111 cryptosporidiosis 9.6
1112 vascular disease 9.6
1113 viral hepatitis 9.6
1114 hepatitis b 9.6
1115 hyperostosis 9.6
1116 ectodermal dysplasia 9.6
1117 thrombocytosis 9.6
1118 keratopathy 9.6
1119 polyclonal hypergammaglobulinemia 9.6
1120 neonatal jaundice 9.6
1121 sick building syndrome 9.6
1122 bilirubin metabolic disorder 9.6
1123 tic disorder 9.6
1124 substance abuse 9.6
1125 proctitis 9.6
1126 lipid metabolism disorder 9.6
1127 bipolar disorder 9.6
1128 histiocytosis 9.6
1129 plague 9.6
1130 mouth disease 9.6
1131 pustulosis of palm and sole 9.6
1132 vasomotor rhinitis 9.6
1133 pancreatitis 9.6
1134 thyroid gland disease 9.6
1135 infertility 9.6
1136 intestinal disease 9.6
1137 lymphopenia 9.6
1138 complement deficiency 9.6
1139 juvenile rheumatoid arthritis 9.6
1140 placenta disease 9.6
1141 septic arthritis 9.6
1142 cataract 9.6
1143 appendicitis 9.6
1144 cyclothymic disorder 9.6
1145 malignant histiocytosis 9.6
1146 seborrheic dermatitis 9.6
1147 rosacea 9.6
1148 amyloidosis 9.6
1149 eczema herpeticum 9.6
1150 diabetes mellitus 9.6
1151 blepharitis 9.6
1152 otitis externa 9.6
1153 bacterial meningitis 9.6
1154 polyarteritis nodosa 9.6
1155 refractive error 9.6
1156 hypoglycemia 9.6
1157 47,xyy 9.6
1158 allergic angiitis 9.6
1159 autoimmune encephalitis 9.6
1160 bronchopulmonary dysplasia 9.6
1161 cold urticaria 9.6
1162 dentinogenesis imperfecta type 2 9.6
1163 eosinophilic cystitis 9.6
1164 giant cell myocarditis 9.6
1165 haemophilus influenzae 9.6
1166 hansen's disease 9.6
1167 lymphomatous thyroiditis 9.6
1168 papular urticaria 9.6
1169 pediatric acute-onset neuropsychiatric syndrome 9.6
1170 prurigo nodularis 9.6
1171 splenomegaly 9.6
1172 depression 9.6
1173 cytomegalovirus infection 9.6
1174 headache 9.6
1175 paresthesia 9.6
1176 seizure disorder 9.6
1177 syncope 9.6
1178 cerebrofacial arteriovenous metameric syndrome 9.6
1179 primary cutaneous lymphoma 9.6
1180 fixed drug eruption 9.6
1181 chronic enteropathy associated with slco2a1 gene 9.6
1182 primary eosinophilic gastrointestinal disease 9.6
1183 systemic polyarteritis nodosa 9.6
1184 solar urticaria 9.6
1185 aniridia 1 9.6
1186 carpal tunnel syndrome 9.6
1187 cornea plana 1, autosomal dominant 9.6
1188 vibratory urticaria 9.6
1189 diabetes mellitus, noninsulin-dependent 9.6
1190 fetal hemoglobin quantitative trait locus 1 9.6
1191 renal cell carcinoma, nonpapillary 9.6
1192 neurofibromatosis, type i 9.6
1193 pernicious anemia 9.6
1194 polykaryocytosis inducer 9.6
1195 actinic prurigo 9.6
1196 porphyria cutanea tarda 9.6
1197 pulmonary hypertension, primary, 1 9.6
1198 small cell cancer of the lung 9.6
1199 thrombocytopenic purpura, autoimmune 9.6
1200 williams-beuren syndrome 9.6
1201 afibrinogenemia, congenital 9.6
1202 cornea plana 2, autosomal recessive 9.6
1203 glycogen storage disease ii 9.6
1204 myelofibrosis 9.6
1205 phenylketonuria 9.6
1206 interstitial pneumonitis, desquamative, familial 9.6
1207 reticulum cell sarcoma 9.6
1208 werner syndrome 9.6
1209 kearns-sayre syndrome 9.6
1210 eukaryotic translation elongation factor 1 alpha-1-like 14 9.6
1211 panbronchiolitis, diffuse 9.6
1212 asthma-related traits 1 9.6
1213 coronary heart disease 1 9.6
1214 mutagen sensitivity 9.6
1215 intraocular pressure quantitative trait locus 9.6
1216 diabetes mellitus, ketosis-prone 9.6
1217 alpha-1-antitrypsin deficiency 9.6
1218 fetal hemoglobin quantitative trait locus 6 9.6
1219 gastric cancer 9.6
1220 barrett esophagus 9.6
1221 leptin deficiency or dysfunction 9.6
1222 leukemia, acute lymphoblastic 3 9.6
1223 hyperprolactinemia 9.6
1224 pachyonychia congenita 3 9.6
1225 dehydrated hereditary stomatocytosis 2 9.6
1226 aspirin allergy 9.6
1227 chlorhexidine allergy 9.6
1228 autoimmune vasculitis 9.6
1229 hemophagocytic lymphohistiocytosis 9.6
1230 restless legs syndrome 9.6
1231 exanthema subitum 9.6
1232 marginal zone b-cell lymphoma 9.6
1233 peripheral t-cell lymphoma 9.6
1234 metabolic acidosis 9.6
1235 hemorrhagic cystitis 9.6
1236 withdrawal disorder 9.6
1237 aphasia 9.6
1238 familial hemiplegic migraine 9.6
1239 scoliosis 9.6
1240 myelomeningocele 9.6
1241 peach allergy 9.6
1242 autosomal dominant nocturnal frontal lobe epilepsy 9.6
1243 lymphoproliferative syndrome 9.6
1244 bone resorption disease 9.6
1245 mucositis 9.6
1246 nodal marginal zone lymphoma 9.6
1247 hypogonadotropic hypogonadism 9.6
1248 cerebral artery occlusion 9.6
1249 thymus lymphoma 9.6
1250 dermatomyositis 9.6
1251 parotitis 9.6
1252 separation anxiety disorder 9.6
1253 mastitis 9.6
1254 portal hypertension 9.6
1255 primary polycythemia 9.6
1256 methemoglobinemia 9.6
1257 gastric ulcer 9.6
1258 hydrocephalus 9.6
1259 amnestic disorder 9.6
1260 impulse control disorder 9.6
1261 corneal edema 9.6
1262 vitamin k deficiency bleeding 9.6
1263 retinal vasculitis 9.6
1264 prediabetes syndrome 9.6
1265 lyme disease 9.6
1266 spinal muscular atrophy 9.6
1267 pathological gambling 9.6
1268 secondary hyperparathyroidism 9.6
1269 hepatic coma 9.6
1270 hemolytic-uremic syndrome 9.6
1271 ancylostomiasis 9.6
1272 dilated cardiomyopathy 9.6
1273 dementia 9.6
1274 pure red-cell aplasia 9.6
1275 tuberous sclerosis 9.6
1276 hyperparathyroidism 9.6
1277 eclampsia 9.6
1278 patent foramen ovale 9.6
1279 facial paralysis 9.6
1280 root caries 9.6
1281 adult-onset still's disease 9.6
1282 shoulder impingement syndrome 9.6
1283 neuroleptic malignant syndrome 9.6
1284 glossitis 9.6
1285 chromoblastomycosis 9.6
1286 heart septal defect 9.6
1287 cheilitis 9.6
1288 mononeuritis multiplex 9.6
1289 atrial heart septal defect 9.6
1290 endodermal sinus tumor 9.6
1291 leiomyosarcoma 9.6
1292 rectum cancer 9.6
1293 hemorrhagic disease 9.6
1294 transient cerebral ischemia 9.6
1295 hidradenitis 9.6
1296 opiate dependence 9.6
1297 benign mesothelioma 9.6
1298 skin atrophy 9.6
1299 glycogen storage disease 9.6
1300 acalculous cholecystitis 9.6
1301 hemoglobinopathy 9.6
1302 testicular cancer 9.6
1303 grade iii astrocytoma 9.6
1304 early myoclonic encephalopathy 9.6
1305 rhabdomyosarcoma 9.6
1306 central nervous system disease 9.6
1307 temporal lobe epilepsy 9.6
1308 coronary aneurysm 9.6
1309 bacterial vaginosis 9.6
1310 choriocarcinoma 9.6
1311 aortic aneurysm 9.6
1312 mast cell neoplasm 9.6
1313 insulinoma 9.6
1314 pancreatic adenocarcinoma 9.6
1315 tick infestation 9.6
1316 coronary stenosis 9.6
1317 hepatitis e 9.6
1318 extracutaneous mastocytoma 9.6
1319 brain edema 9.6
1320 scrapie 9.6
1321 acute t cell leukemia 9.6
1322 retinal disease 9.6
1323 hereditary breast ovarian cancer syndrome 9.6
1324 salpingitis 9.6
1325 paraplegia 9.6
1326 reactive arthritis 9.6
1327 transient hypogammaglobulinemia 9.6
1328 progressive multifocal leukoencephalopathy 9.6
1329 t-cell leukemia 9.6
1330 subacute thyroiditis 9.6
1331 axonal neuropathy 9.6
1332 muscular atrophy 9.6
1333 childhood leukemia 9.6
1334 mite infestation 9.6
1335 ileus 9.6
1336 monocytic leukemia 9.6
1337 viral exanthem 9.6
1338 skin melanoma 9.6
1339 atrophic gastritis 9.6
1340 follicular mucinosis 9.6
1341 albinism 9.6
1342 bap1 tumor predisposition syndrome 9.6
1343 malignant hyperthermia susceptibility 9.6
1344 mitochondrial disorders 9.6
1345 airway-centered interstitial fibrosis 9.6
1346 autoimmune enteropathy 9.6
1347 cerulean cataract 9.6
1348 cluster headache 9.6
1349 eosinophilic pustular folliculitis 9.6
1350 hemiplegic migraine 9.6
1351 hemorrhagic proctocolitis 9.6
1352 mycobacterium fortuitum 9.6
1353 oral cancer 9.6
1354 parainfluenza virus type 3 9.6
1355 pemphigus foliaceus 9.6
1356 pyridoxine deficiency 9.6
1357 soft tissue sarcoma 9.6
1358 sutton disease 2 9.6
1359 brain injury 9.6
1360 fainting 9.6
1361 hypotonia 9.6
1362 pituitary tumors 9.6
1363 postherpetic neuralgia 9.6
1364 audiogenic seizures 9.6
1365 primary peritoneal carcinoma 9.6
1366 secondary interstitial lung disease in childhood and adulthood associated with a connective tissue disease 9.6
1367 low-grade astrocytoma 9.6
1368 rare hereditary hemochromatosis 9.6
1369 combined pulmonary fibrosis-emphysema syndrome 9.6
1370 cutaneous pseudolymphoma 9.6
1371 eosinophilic colitis 9.6
1372 obsolete: squamous cell carcinoma of head and neck 9.6
1373 argyria 9.6
1374 staphylococcal scarlet fever 9.6
1375 discoid lupus erythematosus 9.6
1376 severe immune-mediated enteropathy 9.6
1377 red cell aplasia 9.6
1378 precursor t-cell acute lymphoblastic leukemia 9.6
1379 anorectal anomalies 9.6
1380 complement component 4, partial deficiency of 9.6
1381 creutzfeldt-jakob disease 9.6
1382 ehlers-danlos syndrome, hypermobility type 9.6
1383 lymphoma, mucosa-associated lymphoid type 9.6
1384 kabuki syndrome 1 9.6
1385 lacrimal duct defect 9.6
1386 lymphatic malformation 5 9.6
1387 moebius syndrome 9.6
1388 nail disorder, nonsyndromic congenital, 1 9.6
1389 multiple endocrine neoplasia, type iib 9.6
1390 exfoliation syndrome 9.6
1391 spondylolisthesis 9.6
1392 spondylosis, cervical 9.6
1393 digeorge syndrome 9.6
1394 velocardiofacial syndrome 9.6
1395 argininosuccinic aciduria 9.6
1396 fructose intolerance, hereditary 9.6
1397 hydrocephalus, normal-pressure 9.6
1398 hypogonadism, male 9.6
1399 cartilage-hair hypoplasia 9.6
1400 abnormal hair, joint laxity, and developmental delay 9.6
1401 rheumatic fever-related antigen 9.6
1402 wilson disease 9.6
1403 agammaglobulinemia, x-linked 9.6
1404 congenital hemidysplasia with ichthyosiform erythroderma and limb defects 9.6
1405 reticuloendotheliosis, x-linked 9.6
1406 combined immunodeficiency, x-linked 9.6
1407 craniosynostosis, adelaide type 9.6
1408 intervertebral disc disease 9.6
1409 late-onset retinal degeneration 9.6
1410 diabetes mellitus, permanent neonatal 9.6
1411 patent ductus arteriosus 1 9.6
1412 hypertensive nephropathy 9.6
1413 mevalonic aciduria 9.6
1414 chromosome 16p13.3 deletion syndrome, proximal 9.6
1415 microphthalmia, syndromic 10 9.6
1416 microvascular complications of diabetes 3 9.6
1417 microvascular complications of diabetes 4 9.6
1418 microvascular complications of diabetes 5 9.6
1419 microvascular complications of diabetes 6 9.6
1420 microvascular complications of diabetes 7 9.6
1421 immunodeficiency 9 9.6
1422 pulmonary hypertension, chronic thromboembolic, without deep vein thrombosis 9.6
1423 hypotrichosis and recurrent skin vesicles 9.6
1424 dermatitis, atopic, 9 9.6
1425 psoriasis 14, pustular 9.6
1426 microcephaly, epilepsy, and diabetes syndrome 9.6
1427 mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome 9.6
1428 t-cell receptor-alpha/beta deficiency 9.6
1429 cardiomyopathy, dilated, with woolly hair, keratoderma, and tooth agenesis 9.6
1430 encephalopathy, progressive, with or without lipodystrophy 9.6
1431 chorea, childhood-onset, with psychomotor retardation 9.6
1432 mulchandani-bhoj-conlin syndrome 9.6
1433 speech and communication disorders 9.6
1434 pemphigus gestationis 9.6
1435 japanese spotted fever 9.6
1436 rocky mountain spotted fever 9.6
1437 erysipeloid 9.6
1438 superficial mycosis 9.6
1439 brugada syndrome 9.6
1440 coenzyme q10 deficiency disease 9.6
1441 biotin deficiency 9.6
1442 renal fibrosis 9.6
1443 colorectal adenoma 9.6
1444 follicular lymphoma 9.6
1445 atypical autism 9.6
1446 brain meningioma 9.6
1447 organic acidemia 9.6
1448 ischemic colitis 9.6
1449 lymphocytic colitis 9.6
1450 gallbladder disease 9.6
1451 anal fistula 9.6
1452 fibrous dysplasia 9.6
1453 fibrogenesis imperfecta ossium 9.6
1454 cytomegalovirus retinitis 9.6
1455 cloacal exstrophy 9.6
1456 parotid disease 9.6
1457 purulent acute otitis media 9.6
1458 intestinal atresia 9.6
1459 acute cervicitis 9.6
1460 schizotypal personality disorder 9.6
1461 renal hypertension 9.6
1462 chronic pyelonephritis 9.6
1463 t cell deficiency 9.6
1464 acute hemorrhagic conjunctivitis 9.6
1465 acute orbital inflammation 9.6
1466 social phobia 9.6
1467 functional diarrhea 9.6
1468 laryngostenosis 9.6
1469 listeria meningitis 9.6
1470 dysgammaglobulinemia 9.6
1471 neonatal diabetes mellitus 9.6
1472 synostosis 9.6
1473 optic neuritis 9.6
1474 marasmus 9.6
1475 varicocele 9.6
1476 entropion 9.6
1477 hypertrophic pyloric stenosis 9.6
1478 cyclosporiasis 9.6
1479 choreatic disease 9.6
1480 alcoholic cardiomyopathy 9.6
1481 conduct disorder 9.6
1482 cicatricial entropion 9.6
1483 esophageal candidiasis 9.6
1484 megaloblastic anemia 9.6
1485 trigonitis 9.6
1486 alveolar periostitis 9.6
1487 sapho syndrome 9.6
1488 opisthorchiasis 9.6
1489 autoimmune polyendocrine syndrome 9.6
1490 primary angle-closure glaucoma 9.6
1491 acute retrobulbar neuritis 9.6
1492 pleuropneumonia 9.6
1493 corneal ectasia 9.6
1494 ectropion 9.6
1495 ventricular septal defect 9.6
1496 drug psychosis 9.6
1497 factitious disorder 9.6
1498 pancreas lymphoma 9.6
1499 hepatitis c 9.6
1500 optic nerve disease 9.6
1501 otosalpingitis 9.6
1502 acute maxillary sinusitis 9.6
1503 intestinal perforation 9.6
1504 amelogenesis imperfecta 9.6
1505 spondylosis 9.6
1506 protein s deficiency 9.6
1507 cervicitis 9.6
1508 larynx cancer 9.6
1509 membranoproliferative glomerulonephritis 9.6
1510 inner ear disease 9.6
1511 periarthritis 9.6
1512 wissler's syndrome 9.6
1513 thoracic outlet syndrome 9.6
1514 scleredema adultorum 9.6
1515 oligodendroglioma 9.6
1516 spinal cord disease 9.6
1517 tracheal stenosis 9.6
1518 hyper ige recurrent infection syndrome 1 9.6
1519 benign epilepsy with centrotemporal spikes 9.6
1520 pancreatic ductal adenocarcinoma 9.6
1521 empty sella syndrome 9.6
1522 coronary restenosis 9.6
1523 phototoxic dermatitis 9.6
1524 macular retinal edema 9.6
1525 persian gulf syndrome 9.6
1526 lymph node tuberculosis 9.6
1527 esophagus adenocarcinoma 9.6
1528 eyelid disease 9.6
1529 adenosine deaminase deficiency 9.6
1530 esophageal disease 9.6
1531 transient hypogammaglobulinemia of infancy 9.6
1532 spinal stenosis 9.6
1533 enterobiasis 9.6
1534 active peptic ulcer disease 9.6
1535 laryngeal disease 9.6
1536 mediastinitis 9.6
1537 oropharynx cancer 9.6
1538 decubitus ulcer 9.6
1539 narcolepsy 9.6
1540 mast-cell leukemia 9.6
1541 waardenburg's syndrome 9.6
1542 chronic ethmoiditis 9.6
1543 scotoma 9.6
1544 tracheitis 9.6
1545 chronic cholangitis 9.6
1546 cannabis abuse 9.6
1547 latent syphilis 9.6
1548 ulcerative stomatitis 9.6
1549 biliary tract disease 9.6
1550 intestinal disaccharidase deficiency 9.6
1551 periodontosis 9.6
1552 developmental coordination disorder 9.6
1553 carotenemia 9.6
1554 substance dependence 9.6
1555 cartilage-hair hypoplasia - anauxetic dysplasia spectrum disorders 9.6
1556 actinic cheilitis 9.6
1557 autoimmune inner ear disease 9.6
1558 brittle diabetes 9.6
1559 candida glabrata 9.6
1560 cardiac rupture 9.6
1561 chronic erosive gastritis 9.6
1562 chronic thromboembolic pulmonary hypertension 9.6
1563 congenital cytomegalovirus 9.6
1564 cutaneous mastocytoma 9.6
1565 cutaneous sclerosis 9.6
1566 erythrokeratoderma ''en cocardes'' 9.6
1567 familial colorectal cancer 9.6
1568 hemicrania continua 9.6
1569 insulin-resistance type b 9.6
1570 jackhammer esophagus 9.6
1571 linear lichen planus 9.6
1572 neuromyelitis optica spectrum disorder 9.6
1573 new-onset refractory status epilepticus 9.6
1574 oral leukoplakia 9.6
1575 pediatric multiple sclerosis 9.6
1576 post-transplant lymphoproliferative disease 9.6
1577 recurrent respiratory papillomatosis 9.6
1578 sudden sensorineural hearing loss 9.6
1579 telangiectasia macularis eruptive perstans 9.6
1580 multiple endocrine neoplasia 9.6
1581 angiomatosis 9.6
1582 developmental dyspraxia 9.6
1583 spina bifida cystica 9.6
1584 autoimmune polyendocrinopathy type 4 9.6
1585 acute radiation syndrome 9.6
1586 proton-pump inhibitor-responsive esophageal eosinophilia 9.6
1587 plastic bronchitis 9.6
1588 recurrent acute pancreatitis 9.6
1589 rare genetic skin disease 9.6
1590 striate palmoplantar keratoderma 9.6
1591 aids wasting syndrome 9.6
1592 microtia 9.6
1593 refractory anemia 9.6
1594 aortic aneurysm, familial abdominal, 1 9.5
1595 angelman syndrome 9.5
1596 anisocoria 9.5
1597 arteriovenous malformations of the brain 9.5
1598 central core disease of muscle 9.5
1599 chlorpropamide-alcohol flushing 9.5
1600 orofacial cleft 1 9.5
1601 cleft palate, isolated 9.5
1602 major affective disorder 1 9.5
1603 dermal ridges-off-the-end 9.5
1604 erythermalgia, primary 9.5
1605 factor viii deficiency 9.5
1606 felty syndrome 9.5
1607 fucosidase regulator 9.5
1608 gastritis, familial giant hypertrophic 9.5
1609 glioma susceptibility 1 9.5
1610 diaphragmatic hernia, congenital 9.5
1611 hernia, hiatus 9.5
1612 malignant hyperthermia 1 9.5
1613 keloid formation 9.5
1614 keratosis, familial actinic 9.5
1615 leukemia, acute monocytic 9.5
1616 lipomatosis, multiple 9.5
1617 progressive familial heart block, type ia 9.5
1618 pseudohypoparathyroidism, type ia 9.5
1619 restless legs syndrome 1 9.5
1620 medulloblastoma 9.5
1621 facioscapulohumeral muscular dystrophy 1 9.5
1622 amyotrophy, hereditary neuralgic 9.5
1623 nevus, epidermal 9.5
1624 paroxysmal extreme pain disorder 9.5
1625 benign chronic pemphigus 9.5
1626 phosphatase, acid, of tissues 9.5
1627 pneumothorax, primary spontaneous 9.5
1628 porphyria, acute intermittent 9.5
1629 prader-willi syndrome 9.5
1630 hutchinson-gilford progeria syndrome 9.5
1631 pelvic organ prolapse 9.5
1632 prostate cancer 9.5
1633 ragweed sensitivity 9.5
1634 raynaud disease 9.5
1635 retinal detachment 9.5
1636 odontochondrodysplasia 9.5
1637 supravalvular aortic stenosis 9.5
1638 tetralogy of fallot 9.5
1639 thalassemia, beta+, silent allele 9.5
1640 thyroid cancer, nonmedullary, 2 9.5
1641 tobacco addiction 9.5
1642 torticollis 9.5
1643 tuberous sclerosis 1 9.5
1644 urate oxidase, pseudogene 9.5
1645 muckle-wells syndrome 9.5
1646 cardiomyopathy, familial hypertrophic, 1 9.5
1647 acrodermatitis enteropathica, zinc-deficiency type 9.5
1648 acromesomelic dysplasia, hunter-thompson type 9.5
1649 acth deficiency, isolated 9.5
1650 albinism, oculocutaneous, type ia 9.5
1651 alopecia universalis congenita 9.5
1652 anemia, autoimmune hemolytic 9.5
1653 takayasu arteritis 9.5
1654 asthma, nasal polyps, and aspirin intolerance 9.5
1655 australia antigen 9.5
1656 acth-independent macronodular adrenal hyperplasia 9.5
1657 schopf-schulz-passarge syndrome 9.5
1658 ectodermal dysplasia, hypohidrotic, with hypothyroidism and ciliary dyskinesia 9.5
1659 gastroschisis 9.5
1660 gaucher disease, type i 9.5
1661 monosodium glutamate sensitivity 9.5
1662 multiple acyl-coa dehydrogenase deficiency 9.5
1663 hemolytic uremic syndrome, atypical 1 9.5
1664 hypervitaminosis a 9.5
1665 autoimmune polyendocrine syndrome, type i, with or without reversible metaphyseal dysplasia 9.5
1666 schimke immunoosseous dysplasia 9.5
1667 lymphoid interstitial pneumonia 9.5
1668 microcephaly 1, primary, autosomal recessive 9.5
1669 mitochondrial complex i deficiency, nuclear type 1 9.5
1670 mucopolysaccharidosis, type vi 9.5
1671 epilepsy, myoclonic juvenile 9.5
1672 netherton syndrome 9.5
1673 niemann-pick disease, type c1 9.5
1674 3-methylglutaconic aciduria, type iii 9.5
1675 shwachman-diamond syndrome 1 9.5
1676 pierre robin syndrome 9.5
1677 gitelman syndrome 9.5
1678 pulmonary venoocclusive disease 1, autosomal dominant 9.5
1679 rhabdomyosarcoma 2 9.5
1680 rothmund-thomson syndrome, type 2 9.5
1681 testicular germ cell tumor 9.5
1682 thrombocytopenia 3 9.5
1683 usher syndrome, type iia 9.5
1684 kelley-seegmiller syndrome 9.5
1685 hypophosphatemic rickets, x-linked recessive 9.5
1686 sarcoma, synovial 9.5
1687 angioedema induced by ace inhibitors 9.5
1688 wiskott-aldrich syndrome 9.5
1689 arts syndrome 9.5
1690 hemophilia a 9.5
1691 hemophilia b 9.5
1692 glycerol kinase deficiency 9.5
1693 hypophosphatemic rickets, x-linked dominant 9.5
1694 immunodeficiency with hyper-igm, type 1 9.5
1695 leber optic atrophy 9.5
1696 nuclear ribonucleic acid 9.5
1697 ouabain resistance 9.5
1698 premature ovarian failure 1 9.5
1699 pelizaeus-merzbacher disease 9.5
1700 retinoschisis 1, x-linked, juvenile 9.5
1701 rett syndrome 9.5
1702 spastic paraplegia 2, x-linked 9.5
1703 thrombocytopenia 1 9.5
1704 deafness, nonsyndromic sensorineural, mitochondrial 9.5
1705 mitochondrial myopathy, infantile, transient 9.5
1706 myoclonic epilepsy associated with ragged-red fibers 9.5
1707 exstrophy of bladder 9.5
1708 frontotemporal dementia 9.5
1709 maturity-onset diabetes of the young, type 3 9.5
1710 fryns microphthalmia syndrome 9.5
1711 budd-chiari syndrome 9.5
1712 convulsions, familial infantile, with paroxysmal choreoathetosis 9.5
1713 homocysteinemia 9.5
1714 hyperthyroidism, familial gestational 9.5
1715 ventricular fibrillation, paroxysmal familial, 1 9.5
1716 aceruloplasminemia 9.5
1717 hypertension, early-onset, autosomal dominant, with severe exacerbation in pregnancy 9.5
1718 pars planitis 9.5
1719 aneurysmal bone cysts 9.5
1720 maturity-onset diabetes of the young 9.5
1721 gastrointestinal stromal tumor 9.5
1722 anorexia nervosa 9.5
1723 scheie syndrome 9.5
1724 aortic aneurysm, familial thoracic 1 9.5
1725 spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 1 9.5
1726 bulimia nervosa 9.5
1727 phobia, specific 9.5
1728 legionnaire disease 9.5
1729 lung cancer susceptibility 1 9.5
1730 hyperinsulinemic hypoglycemia, familial, 5 9.5
1731 hyperinsulinemic hypoglycemia, familial, 4 9.5
1732 cortical dysplasia, complex, with other brain malformations 7 9.5
1733 chilblain lupus 1 9.5
1734 leprosy 4 9.5
1735 smoking as a quantitative trait locus 3 9.5
1736 ewing sarcoma 9.5
1737 sarcoidosis 3 9.5
1738 pseudohypoparathyroidism, type ic 9.5
1739 premature ovarian failure 7 9.5
1740 hearing loss, noise-induced 9.5
1741 nijmegen breakage syndrome-like disorder 9.5
1742 purine nucleoside phosphorylase deficiency 9.5
1743 fatty liver disease, nonalcoholic 1 9.5
1744 hermansky-pudlak syndrome 3 9.5
1745 muscle hypertrophy 9.5
1746 delayed sleep phase disorder 9.5
1747 tumor predisposition syndrome 9.5
1748 cerebellar ataxia, neuropathy, and vestibular areflexia syndrome 9.5
1749 alacrima, achalasia, and mental retardation syndrome 9.5
1750 cholangiocarcinoma 9.5
1751 carbonic anhydrase va deficiency, hyperammonemia due to 9.5
1752 robinow syndrome, autosomal dominant 2 9.5
1753 mental retardation, autosomal dominant 43 9.5
1754 lung disease, immunodeficiency, and chromosome breakage syndrome 9.5
1755 phenytoin toxicity 9.5
1756 chronic ulcer of skin 9.5
1757 tendinopathy 9.5
1758 tendinitis 9.5
1759 angiosarcoma 9.5
1760 benzylpenicillin allergy 9.5
1761 phenobarbital allergy 9.5
1762 phenytoin allergy 9.5
1763 sulfamethoxazole allergy 9.5
1764 oxirane allergy 9.5
1765 chlamydia pneumonia 9.5
1766 bacterial sepsis 9.5
1767 hirata disease 9.5
1768 mineral metabolism disease 9.5
1769 dengue shock syndrome 9.5
1770 subcutaneous mycosis 9.5
1771 acute diarrhea 9.5
1772 lambert-eaton myasthenic syndrome 9.5
1773 penicilliosis 9.5
1774 familial adenomatous polyposis 9.5
1775 usher syndrome 9.5
1776 epidemic typhus 9.5
1777 multinodular goiter 9.5
1778 adult t-cell leukemia 9.5
1779 extrapulmonary tuberculosis 9.5
1780 oculocutaneous albinism 9.5
1781 fetal alcohol syndrome 9.5
1782 spastic cerebral palsy 9.5
1783 fetal alcohol spectrum disorder 9.5
1784 anaplastic large cell lymphoma 9.5
1785 zollinger-ellison syndrome 9.5
1786 first-degree atrioventricular block 9.5
1787 second-degree atrioventricular block 9.5
1788 rheumatic heart disease 9.5
1789 oculogyric crisis 9.5
1790 colorectal adenocarcinoma 9.5
1791 extra-adrenal pheochromocytoma 9.5
1792 hereditary ataxia 9.5
1793 cd40 ligand deficiency 9.5
1794 ductal carcinoma in situ 9.5
1795 apraxia 9.5
1796 jejunoileitis 9.5
1797 crohn's colitis 9.5
1798 basal ganglia calcification 9.5
1799 uv-sensitive syndrome 9.5
1800 stuttering 9.5
1801 idiopathic scoliosis 9.5
1802 ptosis 9.5
1803 paroxysmal nocturnal hemoglobinuria 9.5
1804 inguinal hernia 9.5
1805 glucocorticoid-induced osteoporosis 9.5
1806 tomato allergy 9.5
1807 erythema elevatum diutinum 9.5
1808 catecholaminergic polymorphic ventricular tachycardia 9.5
1809 primary autosomal recessive microcephaly 9.5
1810 bone disease 9.5
1811 physical disorder 9.5
1812 cutaneous candidiasis 9.5
1813 hepatic veno-occlusive disease 9.5
1814 superior semicircular canal dehiscence 9.5
1815 non-alcoholic fatty liver disease 9.5
1816 polycystic kidney disease 9.5
1817 non-alcoholic steatohepatitis 9.5
1818 spinocerebellar ataxia type 1 with axonal neuropathy 9.5
1819 migraine with aura 9.5
1820 asymptomatic neurosyphilis 9.5
1821 dysplastic nevus syndrome 9.5
1822 cysticercosis 9.5
1823 venous insufficiency 9.5
1824 optic papillitis 9.5
1825 pleomorphic lipoma 9.5
1826 borderline leprosy 9.5
1827 ehrlichiosis 9.5
1828 left bundle branch hemiblock 9.5
1829 sialadenitis 9.5
1830 asbestosis 9.5
1831 amyotrophic neuralgia 9.5
1832 nasopharyngitis 9.5
1833 orbital granuloma 9.5
1834 osteomalacia 9.5
1835 leukodystrophy 9.5
1836 pleural tuberculosis 9.5
1837 short bowel syndrome 9.5
1838 frontal sinusitis 9.5
1839 dirofilariasis 9.5
1840 st. louis encephalitis 9.5
1841 cholesteatoma of middle ear 9.5
1842 hemiplegia 9.5
1843 ovarian disease 9.5
1844 depersonalization disorder 9.5
1845 leech infestation 9.5
1846 cholecystolithiasis 9.5
1847 miliaria rubra 9.5
1848 pseudomembranous conjunctivitis 9.5
1849 primary hyperparathyroidism 9.5
1850 orbital cellulitis 9.5
1851 arteriovenous malformation 9.5
1852 retinal microaneurysm 9.5
1853 pneumocystosis 9.5
1854 megacolon 9.5
1855 corneal neovascularization 9.5
1856 epidural abscess 9.5
1857 horner's syndrome 9.5
1858 cardiac tamponade 9.5
1859 diabetic autonomic neuropathy 9.5
1860 suppurative otitis media 9.5
1861 hypertensive heart disease 9.5
1862 corneal abscess 9.5
1863 cauda equina syndrome 9.5
1864 hyperandrogenism 9.5
1865 palindromic rheumatism 9.5
1866 gestational diabetes 9.5
1867 emery-dreifuss muscular dystrophy 9.5
1868 choledocholithiasis 9.5
1869 coronary thrombosis 9.5
1870 denture stomatitis 9.5
1871 gastroparesis 9.5
1872 tinea cruris 9.5
1873 conn's syndrome 9.5
1874 panuveitis 9.5
1875 pulmonary alveolar proteinosis 9.5
1876 neurogenic bladder 9.5
1877 alveolar echinococcosis 9.5
1878 otosclerosis 9.5
1879 superficial keratitis 9.5
1880 bile reflux 9.5
1881 paranoid schizophrenia 9.5
1882 male infertility 9.5
1883 alcoholic hepatitis 9.5
1884 bronchopneumonia 9.5
1885 bell's palsy 9.5
1886 pyloric stenosis 9.5
1887 acoustic neuroma 9.5
1888 hereditary hemorrhagic telangiectasia 9.5
1889 newborn respiratory distress syndrome 9.5
1890 diabetic polyneuropathy 9.5
1891 quadriplegia 9.5
1892 keratoconjunctivitis sicca 9.5
1893 mucocele of salivary gland 9.5
1894 lagophthalmos 9.5
1895 plasmodium vivax malaria 9.5
1896 tinea unguium 9.5
1897 focal segmental glomerulosclerosis 9.5
1898 megaesophagus 9.5
1899 endemic goiter 9.5
1900 cutaneous porphyria 9.5
1901 klebsiella pneumonia 9.5
1902 congenital toxoplasmosis 9.5
1903 ehlers-danlos syndrome 9.5
1904 scrub typhus 9.5
1905 hepatic encephalopathy 9.5
1906 neurogenic bowel 9.5
1907 dental fluorosis 9.5
1908 chancroid 9.5
1909 familial hypercholesterolemia 9.5
1910 miliaria 9.5
1911 amenorrhea 9.5
1912 rubeosis iridis 9.5
1913 alcoholic liver cirrhosis 9.5
1914 poems syndrome 9.5
1915 phaeohyphomycosis 9.5
1916 boutonneuse fever 9.5
1917 bacteriuria 9.5
1918 selective igg deficiency disease 9.5
1919 oral candidiasis 9.5
1920 leopard syndrome 9.5
1921 generalized anxiety disorder 9.5
1922 plasmodium malariae malaria 9.5
1923 pyuria 9.5
1924 autosomal dominant cerebellar ataxia 9.5
1925 glossopharyngeal neuralgia 9.5
1926 sclerosing keratitis 9.5
1927 gonadal dysgenesis 9.5
1928 niemann-pick disease 9.5
1929 avoidant personality disorder 9.5
1930 alcohol use disorder 9.5
1931 renovascular hypertension 9.5
1932 endogenous depression 9.5
1933 central nervous system tuberculosis 9.5
1934 mitral valve stenosis 9.5
1935 calcinosis 9.5
1936 childhood absence epilepsy 9.5
1937 gaucher's disease 9.5
1938 hypothalamic disease 9.5
1939 trichomoniasis 9.5
1940 fallopian tube carcinoma 9.5
1941 neuroma 9.5
1942 gestational choriocarcinoma 9.5
1943 autoimmune hepatitis 9.5
1944 b cell deficiency 9.5
1945 enamel caries 9.5
1946 blood platelet disease 9.5
1947 focal epilepsy 9.5
1948 vulvovaginal candidiasis 9.5
1949 motor neuron disease 9.5
1950 craniosynostosis 9.5
1951 acromegaly 9.5
1952 enamel erosion 9.5
1953 hematologic cancer 9.5
1954 splenic infarction 9.5
1955 hemangioma 9.5
1956 transverse colon cancer 9.5
1957 transitional cell carcinoma 9.5
1958 acrodermatitis 9.5
1959 capillary hemangioma 9.5
1960 acute interstitial pneumonia 9.5
1961 acquired polycythemia 9.5
1962 erythropoietin polycythemia 9.5
1963 glucosephosphate dehydrogenase deficiency 9.5
1964 endometrial adenocarcinoma 9.5
1965 aleutian mink disease 9.5
1966 anuria 9.5
1967 breast ductal carcinoma 9.5
1968 malignant glioma 9.5
1969 gliosarcoma 9.5
1970 small cell sarcoma 9.5
1971 acute porphyria 9.5
1972 cutis laxa 9.5
1973 neurilemmoma 9.5
1974 lysosomal storage disease 9.5
1975 lipid pneumonia 9.5
1976 angiomyolipoma 9.5
1977 breast disease 9.5
1978 turner syndrome 9.5
1979 mixed connective tissue disease 9.5
1980 brachial plexus neuritis 9.5
1981 gastric adenocarcinoma 9.5
1982 theileriasis 9.5
1983 vaginal discharge 9.5
1984 granuloma annulare 9.5
1985 pleural empyema 9.5
1986 thrombophlebitis 9.5
1987 vulvitis 9.5
1988 lung squamous cell carcinoma 9.5
1989 acute myocarditis 9.5
1990 thyroid gland follicular carcinoma 9.5
1991 multidrug-resistant tuberculosis 9.5
1992 duodenogastric reflux 9.5
1993 tricuspid valve insufficiency 9.5
1994 biliary dyskinesia 9.5
1995 secondary syphilis 9.5
1996 rh isoimmunization 9.5
1997 pseudohypoparathyroidism 9.5
1998 superficial basal cell carcinoma 9.5
1999 granulomatous dermatitis 9.5
2000 bartter disease 9.5
2001 pseudohypoaldosteronism 9.5
2002 hypokalemia 9.5
2003 embryoma 9.5
2004 rapidly progressive glomerulonephritis 9.5
2005 proliferative glomerulonephritis 9.5
2006 immune-complex glomerulonephritis 9.5
2007 space motion sickness 9.5
2008 adenosquamous carcinoma 9.5
2009 benign ependymoma 9.5
2010 intrahepatic cholangiocarcinoma 9.5
2011 neurotic disorder 9.5
2012 myelodysplastic/myeloproliferative neoplasm 9.5
2013 alcoholic pancreatitis 9.5
2014 optic nerve glioma 9.5
2015 hemangioblastoma 9.5
2016 testicular yolk sac tumor 9.5
2017 colonic disease 9.5
2018 paget's disease of bone 9.5
2019 schizoaffective disorder 9.5
2020 pulmonary venoocclusive disease 9.5
2021 cellular ependymoma 9.5
2022 keratinizing squamous cell carcinoma 9.5
2023 testicular germ cell cancer 9.5
2024 hemoglobinuria 9.5
2025 posterior myocardial infarction 9.5
2026 malignant peripheral nerve sheath tumor 9.5
2027 cerebellar angioblastoma 9.5
2028 adenoma 9.5
2029 cerebrovascular disease 9.5
2030 juvenile pilocytic astrocytoma 9.5
2031 mitochondrial metabolism disease 9.5