Search results for hyperparathyroidism, neonatal severe primary

423 hits were found for hyperparathyroidism, neonatal severe primary

# Family MCID Name MIFTS Score
1
HYP315 Hyperparathyroidism, Neonatal 35 6.993
2
P HYP069 Hyperparathyroidism 58 0.824
3
P HPT021 Hepatitis 69 0.262
4
P THY032 Thyroiditis 54 0.248
5
ADN018 Adenoma 58 0.243
6
P PNC044 Pancreatitis 61 0.229
7
P KDN018 Kidney Disease 66 0.225
8
P HYP086 Hypothyroidism 64 0.219
9
PRT030 Parathyroid Gland Disease 47 0.191
10
PRT029 Parathyroid Adenoma 48 0.191
11
P ART022 Arthritis 75 0.181
12
END072 Endotheliitis 42 0.181
13
NTR005 Nutritional Deficiency Disease 36 0.178
14
P THR014 Thrombocytopenia 64 0.177
15
NRN002 Neuronitis 41 0.175
16
P BRS047 Breast Cancer 100 0.172
17
P LKM002 Leukemia 71 0.169
18
BNS002 Bone Structure Disease 37 0.167
19
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 46 0.166
20
PRT036 Peritonitis 63 0.166
21
P HRT032 Heart Disease 75 0.165
22
P OBS005 Obesity 92 0.157
23
P PNM007 Pneumonia 68 0.156
24
P CHL066 Cholangitis 42 0.153
25
IMP003 Impaired Renal Function Disease 34 0.153
26
P LPS004 Lupus Erythematosus 64 0.145
27
P CRV039 Cervicitis 45 0.144
28
P ADN016 Adenocarcinoma 69 0.144
29
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 36 0.143
30
P NTR004 Neutropenia 59 0.142
31
c CHR089 Chronic Kidney Failure 66 0.142
32
P LVR013 Liver Disease 75 0.142
33
SHR102 Short Stature, Brachydactyly, Intellectual Developmental Disability, and Seizures 43 0.141
34
P FML068 Familial Hypocalciuric Hypercalcemia 46 0.140
35
MLN008 Melanoma 62 0.139
36
P MYP004 Myopathy 67 0.133
37
P RHM011 Rheumatoid Arthritis 89 0.133
38
MDS022 Mediastinitis 41 0.132
39
c ACT027 Acute Pancreatitis 57 0.132
40
ADJ001 Adjustment Disorder 38 0.132
41
P RCK004 Rickets 61 0.129
42
P MYC007 Myocardial Infarction 79 0.125
43
CLT003 Colitis 60 0.124
44
BNC003 Bone Cancer 58 0.123
45
P HYP065 Hyperaldosteronism 50 0.122
46
P MYL005 Myelofibrosis 67 0.122
47
ACR041 Acromelic Frontonasal Dysostosis 45 0.121
48
ALR002 Al-Raqad Syndrome 36 0.121
49
P HYP076 Hyperthyroidism 55 0.121
50
P AMY004 Amyloidosis 65 0.121
51
MTH009 Mouth Disease 61 0.119
52
BRT030 Birth Defects 43 0.119
53
PRS047 Prostatitis 56 0.118
54
END030 End Stage Renal Failure 55 0.118
55
GST050 Gastrointestinal System Disease 56 0.117
56
END035 Endocrine Gland Cancer 49 0.117
57
c PND001 Pain Disorder 54 0.117
58
CNN005 Connective Tissue Disease 62 0.117
59
ACD009 Acid-Labile Subunit, Deficiency of 45 0.116
60
PRP030 Purpura 58 0.113
61
c SYS001 Systemic Lupus Erythematosus 86 0.111
62
ULC004 Ulcerative Colitis 76 0.111
63
NPH003 Nephrocalcinosis 48 0.110
64
CYS001 Cystic Fibrosis 83 0.110
65
c HPT016 Hepatitis B 64 0.109
66
P HYP024 Hypoparathyroidism 53 0.109
67
P URF003 Urofacial Syndrome 1 50 0.109
68
URN009 Urinary System Disease 50 0.109
69
DDN006 Duodenitis 42 0.108
70
P PNC001 Pancytopenia 52 0.108
71
GST045 Gastroenteritis 59 0.108
72
TNP003 Tn Polyagglutination Syndrome, Somatic 41 0.107
73
ART111 Artery Disease 55 0.107
74
PHY002 Physical Disorder 43 0.107
75
PRM097 Primary Immunodeficiency Disease 60 0.106
76
TBR010 Tuberculosis 70 0.106
77
GTR002 Goiter 52 0.105
78
P DRR001 Diarrhea 60 0.105
79
PCK002 Pick Disease 68 0.104
80
P HPT023 Hepatocellular Carcinoma 92 0.103
81
VND001 Vein Disease 47 0.103
82
CNG034 Congestive Heart Failure 72 0.102
83
P NRV007 Nervous System Disease 71 0.101
84
P SPS003 Spastic Diplegia 52 0.100
85
JNT002 Joint Disorders 55 0.100
86
BLD054 Blood Protein Disease 37 0.100
87
LRN003 Learning Disability 49 0.100
88
HYP025 Hyperphosphatemia 47 0.099
89
RNL007 Renal Tubular Acidosis 50 0.099
90
P CNJ013 Conjunctivitis 64 0.098
91
P INF032 Infertility 59 0.098
92
ATH003 Atherosclerosis 65 0.097
93
GRW007 Growth Hormone Deficiency 50 0.096
94
DFC004 Deficiency Anemia 64 0.096
95
NSD001 Nose Disease 48 0.096
96
P AXN010 Axenfeld-Rieger Syndrome, Type 3 55 0.095
97
ALL026 Allergic Hypersensitivity Disease 52 0.095
98
IMM136 Immune System Disease 51 0.095
99
ANX002 Anxiety Disorder 67 0.095
100
LVR012 Liver Cirrhosis 67 0.095
101
P LRY019 Laryngitis 54 0.094
102
VSC011 Vasculitis 62 0.094
103
P CHR345 Chronic Pain 50 0.093
104
P GLM007 Glomerulonephritis 59 0.092
105
c HPT001 Hepatitis C 68 0.092
106
HDN002 Head Injury 45 0.092
107
P APL001 Aplastic Anemia 75 0.091
108
BNF002 Bone Fracture 50 0.091
109
P HYP071 Hypersensitivity Reaction Type Ii Disease 49 0.091
110
P PLY018 Polycythemia 58 0.090
111
ALN001 Aland Island Eye Disease 45 0.090
112
P DBT005 Diabetes Insipidus 53 0.090
113
VGN023 Vaginitis 42 0.089
114
MTB004 Metabolic Acidosis 48 0.089
115
CLC006 Calcinosis 50 0.089
116
P NRV006 Nervous System Cancer 60 0.087
117
URM002 Uremia 48 0.087
118
STM006 Stomach Disease 50 0.087
119
KRT002 Keratomalacia 52 0.087
120
VTM003 Vitamin Metabolic Disorder 30 0.087
121
P HYP060 Hyperinsulinism 58 0.087
122
THY028 Thyroid Cancer 69 0.086
123
P GRV001 Graves' Disease 59 0.085
124
MNR003 Mineral Metabolism Disease 38 0.084
125
P TXP001 Toxoplasmosis 61 0.084
126
P PSD015 Pseudohypoparathyroidism 46 0.084
127
LPD004 Lipoid Nephrosis 48 0.084
128
ACQ007 Acquired Immunodeficiency Syndrome 60 0.083
129
TXC005 Toxic Shock Syndrome 60 0.083
130
LKC003 Leukocyte Disease 43 0.082
131
HYP711 Hypotonia, Ataxia, and Delayed Development Syndrome 26 0.082
132
SPC003 Specific Developmental Disorder 38 0.082
133
P NPH009 Nephrolithiasis 60 0.081
134
c VRL010 Viral Hepatitis 60 0.081
135
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 80 0.081
136
P HMP002 Hemophagocytic Lymphohistiocytosis 64 0.081
137
LPD008 Lipid Metabolism Disorder 58 0.081
138
P PHC003 Pheochromocytoma 71 0.080
139
c SVR003 Severe Congenital Neutropenia 56 0.080
140
BND014 Bone Development Disease 40 0.079
141
ACR002 Acrocapitofemoral Dysplasia 33 0.079
142
P HMN010 Hemangioma 59 0.079
143
BRN002 Bronchiolitis 56 0.079
144
P AST007 Astrocytoma 65 0.078
145
MSC004 Muscle Tissue Disease 34 0.077
146
c TRC078 Trichohepatoenteric Syndrome 2 29 0.077
147
AND005 Androgen Insensitivity Syndrome, Mild 16 0.077
148
P LYM033 Lymphoproliferative Syndrome 56 0.077
149
ALP008 Alopecia 57 0.076
150
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 38 0.076
151
SCK005 Sickle Cell Disease 51 0.076
152
HMT002 Hematologic Cancer 64 0.076
153
KRT006 Keratoconjunctivitis 52 0.075
154
P GLB002 Glioblastoma 68 0.075
155
ART021 Arteriosclerosis 58 0.075
156
OVR063 Overnutrition 50 0.074
157
P CLC005 Celiac Disease 68 0.073
158
SPS057 Spasticity 42 0.073
159
VSC006 Vascular Cancer 51 0.072
160
P GNT008 Giant Cell Tumor 49 0.072
161
P HYP035 Hypophosphatasia 57 0.072
162
PRP080 Peripheral Artery Disease 37 0.072
163
P MMB011 Membranous Nephropathy 54 0.071
164
PHR003 Pharyngitis 56 0.071
165
DWR001 Dwarfism 47 0.071
166
P GLM045 Glioma 60 0.071
167
c PRM225 Primary Thrombocytopenia 39 0.071
168
LYM027 Lymphopenia 56 0.071
169
BNM001 Bone Marrow Cancer 51 0.070
170
HMN014 Human Immunodeficiency Virus Infectious Disease 50 0.070
171
P NRF002 Neurofibromatosis 71 0.069
172
c PNC106 Pancreatic Agenesis 1 37 0.069
173
P MSC033 Muscle Disorders 52 0.069
174
HYP005 Hypokalemia 51 0.069
175
BNM008 Bone Mineral Density, Low 16 0.068
176
P LNG028 Long Qt Syndrome 64 0.068
177
P MCR129 Microvascular Complications of Diabetes 1 54 0.068
178
THR004 Thrombocytosis 55 0.068
179
HPT074 Hepatic Adenoma, Somatic 50 0.068
180
PNC034 Pancreas Disease 58 0.067
181
P GST044 Gastritis 56 0.067
182
P VNS003 Venous Insufficiency 54 0.067
183
ATM012 Autoimmune Disease of Blood 35 0.067
184
ART017 Aortic Disease 57 0.067
185
P PLY019 Polyneuropathy 56 0.066
186
P OST005 Osteogenesis Imperfecta 69 0.066
187
P FNC004 Fanconi Syndrome 49 0.066
188
BRC012 Brucellosis 66 0.066
189
P UVT001 Uveitis 58 0.066
190
PPL002 Papillary Carcinoma 51 0.065
191
CTS003 Coats Disease 57 0.065
192
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 41 0.065
193
P HMR012 Hemorrhagic Fever 56 0.065
194
P ACT135 Acute Graft Versus Host Disease 53 0.064
195
PLM010 Pulmonary Edema 54 0.064
196
GST019 Gastrointestinal Stromal Tumor 73 0.064
197
ADR009 Adrenal Cortex Disease 39 0.064
198
P PYL005 Pyelonephritis 52 0.064
199
FBR054 Fibroma 46 0.064
200
PLM033 Pulmonary Embolism 60 0.064
201
CRB025 Carbohydrate Metabolic Disorder 46 0.063
202
P HRT017 Heart Tumor 32 0.063
203
MYL009 Myelodysplastic Syndrome 73 0.063
204
HRT007 Heart Cancer 46 0.063
205
c ACT071 Acute Kidney Failure 49 0.063
206
P MYC008 Myocarditis 54 0.063
207
SKL014 Skeletal Dysplasia 46 0.063
208
SKL017 Skeletal Dysplasias 45 0.063
209
PRT014 Protein S Deficiency 53 0.063
210
P TBR001 Tuberous Sclerosis 67 0.062
211
GLC003 Glucose Intolerance 55 0.062
212
P TRC086 Trichohepatoenteric Syndrome 1 48 0.062
213
P SPN052 Spondyloarthropathy 60 0.062
214
LST001 Listeriosis 53 0.062
215
MRB003 Morbid Obesity 58 0.062
216
P PLM036 Pulmonary Fibrosis 71 0.061
217
SWL001 Swallowing Disorders 33 0.061
218
APH001 Aphthous Stomatitis 62 0.061
219
P THY023 Thymoma 57 0.061
220
MYX004 Myxedema 35 0.061
221
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 42 0.061
222
P TRN020 Turner Syndrome 65 0.060
223
P HYP192 Hypocalcemia, Autosomal Dominant 56 0.060
224
CNT047 Contact Dermatitis 61 0.060
225
P MYT002 Myotonic Dystrophy 48 0.060
226
URT039 Urticaria 57 0.059
227
P ICH004 Ichthyosis 52 0.059
228
MLT008 Multinodular Goiter 41 0.059
229
CHL004 Cholelithiasis 48 0.058
230
PPL022 Papilloma 55 0.058
231
P PRC031 Preeclampsia/eclampsia 1 51 0.058
232
GRN017 Granulocytopenia 44 0.058
233
VSC047 Vascular Malformation 45 0.058
234
MDL009 Medullary Sponge Kidney 41 0.057
235
P ESS003 Essential Thrombocythemia 70 0.057
236
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 27 0.057
237
MXD005 Mixed Connective Tissue Disease 62 0.057
238
PSR001 Psoriatic Arthritis 64 0.057
239
P ALX003 Alexander Disease 63 0.057
240
BNN003 Bone Inflammation Disease 44 0.057
241
THR100 Thrombocytopenic Purpura, Autoimmune 54 0.057
242
THY030 Thyroid Gland Disease 48 0.057
243
CMM004 Common Variable Immunodeficiency 68 0.057
244
GST023 Gastric Ulcer 56 0.057
245
FBR009 Fibrous Dysplasia 45 0.056
246
c CHR096 Chronic Pulmonary Heart Disease 40 0.056
247
PLM001 Pulmonary Tuberculosis 67 0.056
248
CPL007 Capillary Malformation-Arteriovenous Malformation 40 0.056
249
SFT003 Soft Tissue Sarcoma 57 0.055
250
PRP016 Paraplegia 49 0.055
251
c HMG001 Hemoglobin C Disease 47 0.055
252
P RBL001 Rubella 57 0.055
253
RCT015 Reactive Arthritis 63 0.055
254
P ALP009 Alopecia Areata 62 0.055
255
HYP327 Hypertension, Early-Onset, Autosomal Dominant, with Exacerbation in Pregnancy 33 0.054
256
P DDN001 Duodenal Ulcer 50 0.054
257
P CSH001 Cushing's Syndrome 65 0.054
258
DNG002 Dengue Hemorrhagic Fever 63 0.054
259
ARC002 Arachnoiditis 41 0.054
260
HMN009 Hemangioblastoma 45 0.054
261
APR001 Apraxia 51 0.054
262
P FNC043 Fanconi Anemia, Complementation Group E 55 0.053
263
c ACT073 Acute Leukemia 60 0.053
264
TNS005 Tonsillitis 57 0.053
265
P ACT080 Acute Pulmonary Heart Disease 31 0.052
266
P LPR003 Leprosy 69 0.052
267
SLV003 Salivary Gland Disease 47 0.052
268
CRN265 Craniofacial Malformations, Asymmetric, with Polysyndactyly and Abnormal Skin and Gut Development 33 0.052
269
PHS001 Phosphorus Metabolism Disease 38 0.052
270
BCL002 B Cell Deficiency 49 0.052
271
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 48 0.051
272
LRY017 Laryngeal Disease 34 0.051
273
IRN001 Iron Deficiency Anemia 52 0.051
274
RFR010 Refractory Anemia 45 0.051
275
CNT046 Central Nervous System Vasculitis 46 0.051
276
MLT077 Multiple Sclerosis, Disease Progression, Modifier of 78 0.051
277
P PRC019 Precocious Puberty 51 0.050
278
LCT002 Lactose Intolerance 46 0.050
279
ORL015 Oral Squamous Cell Carcinoma 57 0.050
280
LPD007 Lipoadenoma 29 0.050
281
P ART034 Aortopulmonary Window 23 0.050
282
c CHR431 Chronic Venous Insufficiency 44 0.050
283
c HPT007 Hepatitis E 54 0.050
284
IMP004 Impetigo 42 0.050
285
PRR002 Pure Red-Cell Aplasia 47 0.050
286
ECH003 Echinococcosis 54 0.049
287
MYC002 Mycobacterium Avium Complex Disease 52 0.049
288
ADR005 Adrenal Carcinoma 57 0.049
289
CCC002 Coccidiosis 51 0.049
290
RNL097 Renal Artery Disease 43 0.049
291
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 43 0.049
292
VTM002 Vitamin B12 Deficiency 44 0.048
293
KRT008 Keratopathy 44 0.048
294
P UVL004 Uveal Melanoma 60 0.048
295
RNL078 Renal Dysplasia 45 0.048
296
PRN021 Paranasal Sinus Disease 49 0.048
297
NDL007 Nodular Goiter 46 0.048
298
PMS001 Poems Syndrome 52 0.047
299
PLY125 Polycythemia Vera, Somatic 63 0.047
300
RHM028 Rheumatic Heart Disease 50 0.047
301
OMN001 Omenn Syndrome 67 0.047
302
P PNV001 Panuveitis 50 0.047
303
PRN011 Pernicious Anemia 44 0.047
304
c BRN108 Branchiootic Syndrome 1 34 0.047
305
GLM004 Gliomatosis Cerebri 49 0.047
306
ECT004 Ecthyma 35 0.046
307
c NRF018 Neurofibromatosis, Type 1 67 0.046
308
HMR004 Hemorrhagic Fever with Renal Syndrome 58 0.046
309
BRN012 Bronchiolitis Obliterans 58 0.046
310
P PLM006 Pulmonary Alveolar Proteinosis 48 0.046
311
ARC007 Arachnoid Cysts 39 0.045
312
P MYM002 Moyamoya Disease 61 0.045
313
P LRY044 Larynx Cancer 57 0.045
314
HST011 Histoplasmosis 52 0.045
315
ISL001 Islet Cell Tumor 50 0.045
316
END038 Endocrine Pancreas Disease 41 0.045
317
KLN001 Klinefelter's Syndrome 50 0.045
318
HYP068 Hyperostosis 40 0.045
319
c HMG004 Hemoglobin D Disease 31 0.045
320
HYP063 Hypersplenism 48 0.044
321
CMP010 Complex Regional Pain Syndrome 54 0.044
322
PNN001 Panniculitis 51 0.044
323
VSC044 Visceral Myopathy 51 0.044
324
RLP002 Relapsing-Remitting Multiple Sclerosis 55 0.044
325
P LCH002 Lichen Planus 53 0.044
326
SPS019 Spastic Paraparesis 41 0.044
327
c FML303 Familial/multiple Cancer 14 0.043
328
ESN011 Eisenmenger Syndrome 45 0.043
329
MCR088 Microscopic Polyangiitis 49 0.043
330
P ART084 Arteriovenous Fistula 44 0.043
331
VSC003 Visceral Leishmaniasis 56 0.043
332
ABL002 Ablepharon-Macrostomia Syndrome 57 0.043
333
FLL031 Follicular Adenoma 42 0.043
334
c SRC025 Sarcoidosis 1 61 0.042
335
CYS039 Cystic Kidney Disease 52 0.042
336
P PNL012 Penile Cancer 58 0.042
337
P MNC007 Monocytic Leukemia 55 0.042
338
c ANT034 Anterior Uveitis 48 0.042
339
TRY001 Trypanosomiasis 51 0.042
340
DNG001 Dengue Shock Syndrome 43 0.041
341
P PNM006 Pneumoconiosis 51 0.041
342
P SML016 Small Intestine Cancer 52 0.041
343
CYS013 Cystinuria 63 0.041
344
ALL010 Allergic Contact Dermatitis 57 0.040
345
TKY002 Takayasu Arteritis 61 0.040
346
CHR063 Chronic Mucocutaneous Candidiasis 63 0.040
347
END028 Endemic Goiter 35 0.040
348
P MDL022 Medullary Thyroid Carcinoma, Familial 63 0.040
349
STR072 Stromal Keratitis 46 0.040
350
P ACT150 Acute Adrenal Insufficiency 45 0.040
351
P ESN008 Eosinophilic Pneumonia 51 0.040
352
LWS003 Lowe Syndrome 61 0.040
353
P GCH001 Gaucher's Disease 62 0.039
354
PST053 Postherpetic Neuralgia 40 0.039
355
P BRC006 Brachydactyly 54 0.039
356
c SPN225 Spondyloarthropathy 1 62 0.039
357
c PRM023 Pre-Malignant Neoplasm 41 0.039
358
NPH004 Nephropathia Epidemica 40 0.039
359
EXT034 Extrinsic Allergic Alveolitis 54 0.039
360
P ATX010 Ataxia Neuropathy Spectrum 30 0.039
361
IDP064 Idiopathic Neutropenia 45 0.039
362
SQM013 Squamous Cell Carcinoma, Head and Neck 70 0.038
363
MCR191 Microscopic Colitis 47 0.038
364
c ART106 Arterial Calcification, Generalized, of Infancy, 1 39 0.038
365
ALK013 Alkaptonuria 54 0.038
366
c ATM022 Autoimmune Myocarditis 42 0.038
367
CHY002 Chylomicron Retention Disease 57 0.038
368
HSH003 Hashimoto Thyroiditis 62 0.037
369
ALP001 Alopecia Universalis 58 0.037
370
P DYS007 Dyskeratosis Congenita 63 0.037
371
c INT064 Intermediate Uveitis 52 0.037
372
SLC006 Silicosis 53 0.037
373
PTT037 Pituitary Tumors 45 0.037
374
c MCR113 Microvascular Complications of Diabetes 3 45 0.037
375
RNL077 Renal Fibrosis 47 0.037
376
ELS001 Eales Disease 47 0.037
377
CTN007 Cutaneous Leishmaniasis 62 0.036
378
LCH004 Lichen Disease 36 0.036
379
ALV002 Alveolar Echinococcosis 46 0.036
380
RGH009 Right Atrial Isomerism 44 0.036
381
c CNG124 Congenital Rubella 44 0.036
382
EXN001 Exanthema Subitum 39 0.036
383
c GRV008 Graves Disease 1 44 0.036
384
CYS010 Cystinosis 53 0.036
385
NTR040 Neutropenia, Cyclic 51 0.036
386
ERY017 Erythema Elevatum Diutinum 49 0.036
387
SCL022 Scleredema 32 0.035
388
EXT035 Extrinsic Cardiomyopathy 37 0.035
389
CRD003 Cardiac Sarcoidosis 42 0.035
390
MGK001 Megakaryocytic Leukemia 55 0.035
391
MCC002 Mucocutaneous Leishmaniasis 46 0.035
392
RSP002 Respiratory Syncytial Virus Infectious Disease 46 0.035
393
IRT001 Iritis 34 0.035
394
CRV030 Cervical Adenitis 30 0.035
395
CRR007 Cirrhosis, Cryptogenic 43 0.034
396
ANC002 Anca-Associated Vasculitis 42 0.034
397
P LKM068 Leukemia, Chronic Myeloid, Somatic 68 0.034
398
P HYP057 Hypervitaminosis D 38 0.033
399
PTY001 Pityriasis Rosea 42 0.033
400
CHR286 Chronic Neutrophilic Leukemia 43 0.032
401
PLM032 Pulmonary Blastoma 49 0.032
402
TRC006 Trichosporonosis 29 0.032
403
OPP002 Opportunistic Mycosis 41 0.032
404
ORF044 Orofacial Granulomatosis 37 0.032
405
CWM001 Cow Milk Allergy 40 0.032
406
c HYP273 Hypothyroidism, Congenital, Due to Thyroid Dysgenesis or Hypoplasia 49 0.032
407
INH011 Inherited Bone Marrow Failure Syndromes 27 0.032
408
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 26 0.032
409
c CHR576 Chronic Beryllium Disease 41 0.031
410
GRN009 Granulomatous Hepatitis 39 0.031
411
P RFR008 Refractory Anemia with Excess Blasts 31 0.031
412
BRT005 Barth Syndrome 52 0.031
413
NRW001 Norwegian Scabies 42 0.031
414
P KNN002 Kenny-Caffey Syndrome 41 0.031
415
ESN004 Eosinophilic Gastritis 41 0.030
416
VGT001 Vogt-Koyanagi-Harada Disease 54 0.030
417
LKM066 Leukemia, Acute Myelomonocytic, Somatic, Somatic 60 0.030
418
THY103 Thyroid Cancer, Monmedullary, 1 53 0.030
419
CYC007 Cyclic Thrombocytopenia 37 0.030
420
CMP052 Complication in Hemodialysis 13 0.029
421
P TRC072 Treacher Collins Syndrome 1 52 0.029
422
P THY102 Thyroid Cancer, Nonmedullary, 2 58 0.028
423
PRS012 Pars Planitis 43 0.026
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