Search results for NSF

403 hits were found for NSF

# Family MCID Name MIFTS Score
1
NPH018 Nephrogenic Systemic Fibrosis 48 22.208
2
TTN003 Tetanus 64 16.950
3
P SCH015 Schizophrenia 74 14.816
4
P ERL057 Early Infantile Epileptic Encephalopathy 61 9.286
5
NRN008 Neuronal Intranuclear Inclusion Disease 45 9.165
6
c TYP037 Type 1 Diabetes Mellitus 13 20 8.333
7
TNG001 Tungiasis 40 8.333
8
c LKD019 Leukodystrophy, Hypomyelinating, 6 52 8.333
9
SYN089 Syndromic X-Linked Intellectual Disability Snyder Type 37 8.333
10
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 4.638
11
PLY150 Polykaryocytosis Inducer 29 3.131
12
END086 End Stage Renal Disease 54 2.194
13
c ACT071 Acute Kidney Failure 60 2.141
14
c CHR684 Chronic Kidney Disease 73 1.916
15
P CRN300 Coronary Heart Disease 1 73 1.701
16
P TMP001 Temporal Lobe Epilepsy 49 1.664
17
P KDN018 Kidney Disease 71 1.563
18
c PLM164 Pulmonary Hypertension, Primary, 1 75 1.547
19
TRN015 Transient Cerebral Ischemia 62 1.505
20
ISC004 Ischemia 61 1.442
21
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 1.316
22
SKN016 Skin Disease 63 1.315
23
P RTN008 Retinitis Pigmentosa 79 1.304
24
NRR001 Neuroretinitis 42 1.304
25
RTN023 Retinitis 45 1.304
26
ART002 Arts Syndrome 66 1.126
27
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 1.074
28
HMS001 Hemosiderosis 48 1.074
29
INS001 Insulinoma 59 1.074
30
P ADL010 Adult Respiratory Distress Syndrome 70 1.074
31
P RRH023 Rare Hereditary Hemochromatosis 52 1.074
32
P SYS005 Systemic Scleroderma 73 1.035
33
CRB079 Cerebrospinal Fluid Leak 35 1.035
34
INC018 Inclusion Body Myopathy with Paget Disease of Bone and Frontotemporal Dementia 51 1.031
35
CCN001 Cocaine Dependence 47 1.031
36
P ENC018 Encephalopathy 62 0.982
37
PPL052 Papillomatosis, Confluent and Reticulated 34 0.921
38
c SCL052 Scleroderma, Familial Progressive 60 0.898
39
P EPL164 Epilepsy 70 0.898
40
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.882
41
P HDC001 Headache 56 0.882
42
P ATS364 Autism 72 0.853
43
P MSC005 Muscular Dystrophy 66 0.832
44
SPN186 Spinal Cord Injury 60 0.832
45
SCL025 Scleromyxedema 37 0.830
46
NPH009 Nephrolithiasis 54 0.775
47
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.760
48
FBR047 Fibromyalgia 57 0.760
49
HYP025 Hyperphosphatemia 47 0.756
50
P BRS047 Breast Cancer 97 0.753
51
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.711
52
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 38 0.711
53
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 36 0.711
54
LTN004 Late-Onset Retinal Degeneration 59 0.711
55
c BRN108 Branchiootic Syndrome 1 63 0.711
56
c MYS033 Miyoshi Muscular Dystrophy 1 53 0.711
57
DSS008 Disease of Mental Health 74 0.711
58
P MYP004 Myopathy 67 0.711
59
P LMB006 Limb-Girdle Muscular Dystrophy 52 0.711
60
P PNC035 Pancreatic Cancer 87 0.704
61
MTB004 Metabolic Acidosis 48 0.674
62
c DWL002 Dowling-Degos Disease 1 58 0.663
63
P PTT006 Pituitary Adenoma 55 0.617
64
KLD004 Keloid Disorder 38 0.593
65
ADN018 Adenoma 58 0.581
66
P HRT032 Heart Disease 84 0.581
67
CRN036 Craniopharyngioma 63 0.581
68
P HYP069 Hyperparathyroidism 62 0.568
69
DNT012 Dental Caries 53 0.568
70
INC021 Incontinentia Pigmenti 63 0.533
71
P AST005 Asthma 75 0.533
72
ANX010 Anxiety 70 0.528
73
STM007 Stomatitis 52 0.528
74
c OGC001 Oguchi Disease 1 39 0.514
75
P SZR006 Seizure Disorder 69 0.514
76
P OGC005 Oguchi Disease 44 0.514
77
NPH091 Nephrolithiasis, Calcium Oxalate 61 0.499
78
HPT014 Hepatorenal Syndrome 49 0.499
79
PLR007 Pleural Empyema 50 0.499
80
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 44 0.469
81
PTT037 Pituitary Tumors 44 0.469
82
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 0.453
83
P LVR013 Liver Disease 68 0.453
84
HYP066 Hyperglycemia 60 0.453
85
c PRM005 Primary Hyperparathyroidism 59 0.453
86
P ERY036 Erythema Nodosum 49 0.453
87
P GRF003 Graft-Versus-Host Disease 71 0.437
88
ALL029 Allergic Disease 61 0.437
89
CTN020 Cutaneous Sclerosis 16 0.437
90
P OVR082 Overgrowth Syndrome 41 0.437
91
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 0.419
92
SCL002 Scleredema Adultorum 45 0.419
93
c LCL006 Localized Scleroderma 64 0.419
94
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 0.402
95
HYP457 Hypertrophic Scars 42 0.402
96
P GST044 Gastritis 55 0.402
97
MDD011 Mood Disorder 61 0.402
98
URL001 Urolithiasis 45 0.402
99
P HML001 Hemolytic-Uremic Syndrome 52 0.402
100
P RTN016 Retinal Degeneration 52 0.402
101
P NGH001 Night Blindness 52 0.402
102
c MJR022 Major Affective Disorder 8 37 0.383
103
P SLP006 Sleep Apnea 69 0.383
104
STR067 Stroke, Ischemic 79 0.383
105
c MJR024 Major Affective Disorder 9 40 0.383
106
ESP021 Esophageal Cancer 84 0.383
107
RPD005 Rapidly Involuting Congenital Hemangioma 48 0.383
108
P BPL003 Bipolar Disorder 56 0.383
109
RTC003 Root Caries 33 0.383
110
MSL004 Mesial Temporal Lobe Epilepsy with Hippocampal Sclerosis 26 0.383
111
DPR016 Depression 64 0.383
112
P CHR345 Chronic Pain 50 0.383
113
ESN015 Eosinophilic Fasciitis 46 0.363
114
P NSP012 Nasopharyngeal Carcinoma 60 0.363
115
P MNN007 Meningocele 39 0.363
116
P INF032 Infertility 60 0.363
117
FSC004 Fasciitis 49 0.363
118
IDP073 Idiopathic Hypercalciuria 41 0.363
119
DYS073 Dysphagia 53 0.363
120
P SCL018 Scoliosis 57 0.343
121
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 0.343
122
DSS032 Disease by Infectious Agent 55 0.343
123
MNN043 Meningioma, Familial 79 0.343
124
P RSP003 Respiratory Failure 73 0.343
125
LYM002 Lymphoplasmacyte-Rich Meningioma 35 0.343
126
SCR001 Secretory Meningioma 40 0.343
127
CLC001 Calciphylaxis 50 0.343
128
INT395 Intracranial Meningioma 47 0.343
129
TBR007 Tuberculum Sellae Meningioma 28 0.343
130
PRT036 Peritonitis 65 0.343
131
IDP070 Idiopathic Scoliosis 41 0.320
132
P ALZ034 Alzheimer Disease 87 0.320
133
P SCL057 Scoliosis, Isolated 1 40 0.320
134
P LNG032 Lung Cancer 98 0.320
135
P LNG064 Lung Cancer Susceptibility 3 69 0.320
136
ANK001 Ankylosis 50 0.320
137
PST028 Post-Traumatic Stress Disorder 58 0.320
138
SVR004 Severe Combined Immunodeficiency 70 0.320
139
FRZ001 Frozen Shoulder 54 0.320
140
BRS064 Bursitis 51 0.320
141
P RTN018 Retinal Disease 53 0.320
142
P HYP083 Hypopituitarism 51 0.320
143
P NRB001 Neuroblastoma 66 0.320
144
ORL011 Oral Cancer 60 0.320
145
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 0.297
146
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 0.297
147
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.297
148
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 0.297
149
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.297
150
KPS004 Kaposi Sarcoma 76 0.297
151
c ART101 Aortic Valve Disease 2 65 0.297
152
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 0.297
153
c BDY019 Body Mass Index Quantitative Trait Locus 18 46 0.297
154
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.297
155
P LKM071 Leukemia, Chronic Lymphocytic 74 0.297
156
P HYP726 Hypercalcemia, Infantile, 1 58 0.297
157
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.297
158
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.297
159
P CTS001 Cutis Laxa 64 0.297
160
CHL014 Cholera 62 0.297
161
NPH003 Nephrocalcinosis 49 0.297
162
P BCL017 B-Cell Lymphoma 57 0.297
163
GLM045 Glioma 62 0.297
164
GLL048 Glial Tumor 51 0.297
165
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 0.271
166
P BDY004 Body Mass Index Quantitative Trait Locus 11 82 0.271
167
HYP798 Hypophosphatemic Rickets, X-Linked Recessive 60 0.271
168
PRP027 Peripheral Vascular Disease 71 0.271
169
P RST001 Restless Legs Syndrome 52 0.271
170
INT017 Intestinal Schistosomiasis 51 0.271
171
KLD003 Keloid Formation 34 0.271
172
c AMY091 Amyotrophic Lateral Sclerosis 1 87 0.271
173
CMB007 Combined Immunodeficiency 56 0.271
174
ENM001 Enamel Caries 28 0.271
175
P DRR001 Diarrhea 55 0.271
176
P DYS005 Dyslexia 40 0.271
177
P INT068 Intestinal Disease 53 0.271
178
P LTR001 Lateral Sclerosis 57 0.271
179
RYS001 Reye Syndrome 49 0.271
180
P PRR002 Pure Red-Cell Aplasia 46 0.271
181
SVR001 Severe Acute Respiratory Syndrome 68 0.271
182
SPN035 Spindle Cell Sarcoma 51 0.271
183
OST011 Osteomalacia 52 0.271
184
DNT010 Dentin Caries 32 0.271
185
RCK004 Rickets 64 0.271
186
CVD001 Covid-19 59 0.271
187
MNT002 Mental Depression 56 0.271
188
SCH014 Schistosomiasis 56 0.271
189
SRC014 Sarcoma 64 0.271
190
ACT084 Acute Stress Disorder 53 0.271
191
LRN003 Learning Disability 49 0.271
192
ONC003 Oncogenic Osteomalacia 42 0.271
193
JVN033 Juvenile Nasopharyngeal Angiofibroma 45 0.271
194
MLR004 Malaria 77 0.242
195
P CRD119 Cardiac Arrest 68 0.242
196
OPP004 Oppositional Defiant Disorder 48 0.242
197
ATH013 Atherosclerosis Susceptibility 63 0.242
198
DWN001 Down Syndrome 70 0.242
199
HND015 Hand Skill, Relative 29 0.242
200
HLX001 Helix Syndrome 47 0.242
201
FDB001 Foodborne Botulism 55 0.242
202
MYL069 Myeloma, Multiple 76 0.242
203
P MJR001 Major Depressive Disorder 68 0.242
204
P PRK057 Parkinson Disease, Late-Onset 79 0.242
205
P PHC003 Pheochromocytoma 70 0.242
206
ADR040 Adrenal Gland Pheochromocytoma 45 0.242
207
GST023 Gastric Ulcer 52 0.242
208
P BNC003 Bone Cancer 58 0.242
209
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 0.242
210
P KDN017 Kidney Cancer 60 0.242
211
P RHN004 Rhinitis 56 0.242
212
PSY004 Psychotic Disorder 66 0.242
213
P HYD006 Hydrocephalus 62 0.242
214
c BPL002 Bipolar I Disorder 47 0.242
215
P URT039 Urticaria 57 0.242
216
PRT037 Pertussis 49 0.242
217
CRB004 Cerebral Artery Occlusion 45 0.242
218
GT001 Gout 63 0.242
219
OLF005 Olfactory Neuroblastoma 46 0.242
220
c ACT075 Acute Myocardial Infarction 55 0.242
221
CYT002 Cytokine Deficiency 43 0.242
222
ETN001 Eating Disorder 59 0.242
223
48X005 48,xyyy 39 0.242
224
P ENC008 Encephalocele 46 0.242
225
CLT003 Colitis 63 0.210
226
APH002 Aphasia 55 0.210
227
CHR072 Chordoma 56 0.210
228
GST092 Gastroesophageal Reflux 59 0.210
230
P PLM037 Pulmonary Hypertension 69 0.210
231
ARC025 Arachnoid Cysts, Intracranial 37 0.210
232
FRN006 Frontotemporal Dementia 68 0.210
233
P MYC007 Myocardial Infarction 69 0.210
234
c LFR007 Li-Fraumeni Syndrome 2 45 0.210
235
CTN028 Cutaneous Telangiectasia and Cancer Syndrome, Familial 70 0.210
236
P TMR010 Tumor Predisposition Syndrome 69 0.210
237
P DNG005 Dengue Virus 55 0.210
238
P HNT016 Huntington Disease 73 0.210
239
P LFR001 Li-Fraumeni Syndrome 73 0.210
240
P SPR120 Supranuclear Palsy, Progressive, 1 68 0.210
241
c LFR009 Li-Fraumeni Syndrome 1 32 0.210
242
P VNT002 Ventricular Septal Defect 58 0.210
243
FCL014 Focal Epilepsy 53 0.210
244
NRT004 Neuritis 53 0.210
245
HRT011 Heart Septal Defect 49 0.210
246
HMP001 Hemopericardium 47 0.210
247
P ALC033 Alcohol Use Disorder 67 0.210
248
CNG034 Congestive Heart Failure 69 0.210
249
P CNJ013 Conjunctivitis 66 0.210
250
MTR002 Mitral Valve Insufficiency 51 0.210
251
P EHL001 Ehlers-Danlos Syndrome 57 0.210
252
P GLM007 Glomerulonephritis 59 0.210
253
TRC022 Tricuspid Valve Insufficiency 46 0.210
254
CRC021 Carcinosarcoma 62 0.210
255
P SBS003 Substance Abuse 54 0.210
256
P PRC012 Pericardial Effusion 50 0.210
257
KHN001 Kuhnt-Junius Degeneration 48 0.210
258
P DMN002 Dementia 65 0.210
259
TLN003 Telangiectasis 51 0.210
260
P SLP005 Sleep Disorder 61 0.210
261
CHR178 Chromosomal Triplication 33 0.210
262
CRT033 Corticobasal Degeneration 48 0.210
263
DRG003 Drug Dependence 46 0.210
264
TRM010 Traumatic Brain Injury 50 0.210
265
RCR030 Recurrent Idiopathic Neuroretinitis 11 0.210
266
CBP002 Cebpe-Associated Autoinflammation-Immunodeficiency-Neutrophil Dysfunction Syndrome 18 0.210
267
FBR085 Fibrillary Glomerulonephritis 25 0.210
268
INH023 Inherited Cancer-Predisposing Syndrome 53 0.210
269
P FBR031 Febrile Seizures 52 0.210
270
STT041 Stuttering 52 0.171
271
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 0.171
272
ATR057 Atrioventricular Block 54 0.171
273
c MGR028 Migraine with or Without Aura 1 63 0.171
274
P PRS040 Prostate Cancer 95 0.171
275
c SML038 Small Cell Cancer of the Lung 68 0.171
276
TBC004 Tobacco Addiction 63 0.171
277
ALC007 Alcohol Dependence 65 0.171
278
SPP012 Suppressor of Tumorigenicity 11 19 0.171
279
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 0.171
280
c MCR133 Microvascular Complications of Diabetes 4 41 0.171
281
c MCR113 Microvascular Complications of Diabetes 3 52 0.171
282
c MCR130 Microvascular Complications of Diabetes 6 41 0.171
283
c MCR120 Microvascular Complications of Diabetes 7 47 0.171
284
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.171
285
c TYP008 Type 1 Diabetes Mellitus 77 0.171
286
DRR016 Diarrhea 2, with Microvillus Atrophy 55 0.171
287
c 46X049 46,xy Sex Reversal 2 51 0.171
288
FBR012 Fabry Disease 71 0.171
289
EPD052 Epidermolysis Bullosa Simplex Superficialis 17 0.171
290
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 0.171
291
APN008 Apnea, Obstructive Sleep 66 0.171
292
ATM095 Autoimmune Disease 61 0.171
293
c PRG042 Progressive Familial Heart Block, Type Ia 65 0.171
294
CRV035 Cervical Cancer 72 0.171
295
P SMK004 Smoking As a Quantitative Trait Locus 3 44 0.171
296
GLB002 Glioblastoma 67 0.171
297
PLM029 Palmoplantar Keratosis 48 0.171
298
P VSC007 Vascular Disease 62 0.171
299
P ICH004 Ichthyosis 56 0.171
300
P OTS001 Otosclerosis 49 0.171
301
ART017 Aortic Disease 49 0.171
302
AMN001 Amenorrhea 53 0.171
303
P HYP086 Hypothyroidism 68 0.171
304
c SCN007 Secondary Hyperparathyroidism 50 0.171
305
SCL003 Social Phobia 48 0.171
306
LFT001 Left Bundle Branch Hemiblock 47 0.171
307
DNG002 Dengue Hemorrhagic Fever 59 0.171
308
P VSC011 Vasculitis 61 0.171
309
P MYL006 Myeloid Leukemia 60 0.171
310
SBS004 Substance Dependence 46 0.171
311
CLF001 Cleft Lip 54 0.171
312
FTT001 Fatty Liver Disease 61 0.171
313
PST021 Postpartum Depression 50 0.171
314
CRH001 Crohn's Disease 80 0.171
315
P HYP098 Hypereosinophilic Syndrome 66 0.171
316
ESN002 Eosinophilia-Myalgia Syndrome 40 0.171
317
INT075 Intracranial Hypertension 52 0.171
319
TXC020 Toxic Oil Syndrome 33 0.171
320
BRN071 Brain Injury 50 0.171
321
c ATS007 Autism Spectrum Disorder 71 0.121
322
BDY001 Body Dysmorphic Disorder 40 0.121
323
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 0.121
324
RNL077 Renal Fibrosis 46 0.121
325
ERY003 Erythema Multiforme 56 0.121
326
WLL001 Williams-Beuren Syndrome 60 0.121
327
P OVR042 Ovarian Cancer 88 0.121
328
NRL016 Neural Tube Defects 80 0.121
329
P RTN024 Retinoblastoma 72 0.121
330
OCL069 Ocular Motor Apraxia 57 0.121
331
c MCP043 Mucopolysaccharidosis, Type Iiia 60 0.121
332
TRP006 Tarp Syndrome 58 0.121
333
P BLD134 Bladder Cancer 79 0.121
334
OST159 Osteogenic Sarcoma 66 0.121
335
c HMP022 Hemophagocytic Lymphohistiocytosis, Familial, 1 65 0.121
336
P CLR023 Colorectal Cancer 100 0.121
337
P MLT020 Multiple Sclerosis 79 0.121
338
c LKM061 Leukemia, Acute Myeloid 83 0.121
339
c HMP014 Hemophagocytic Lymphohistiocytosis, Familial, 4 49 0.121
340
AGN016 Aging 53 0.121
341
NRD093 Neurodevelopmental Disorder with Epilepsy, Spasticity, and Brain Atrophy 19 0.121
342
P HMP002 Hemophagocytic Lymphohistiocytosis 60 0.121
343
CRB069 Cerebral Dysgenesis, Neuropathy, Ichthyosis, and Palmoplantar Keratoderma Syndrome 47 0.121
344
c PRK058 Parkinson Disease 16 18 0.121
345
P GST053 Gastric Cancer 82 0.121
346
CHP002 Chops Syndrome 47 0.121
347
SZR028 Seizures, Scoliosis, and Macrocephaly/microcephaly Syndrome 36 0.121
348
P MCP040 Mucopolysaccharidosis-Plus Syndrome 70 0.121
349
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 58 0.121
350
c LKM063 Leukemia, Chronic Myeloid 70 0.121
351
SVR097 Severe Cutaneous Adverse Reaction 68 0.121
352
c OPT053 Optic Atrophy 1 62 0.121
353
RNL114 Renal Cell Carcinoma, Nonpapillary 79 0.121
354
CLF027 Cleft Palate, Isolated 64 0.121
355
P HPT023 Hepatocellular Carcinoma 95 0.121
356
BNR002 Bone Resorption Disease 47 0.121
357
RBS001 Rabies 57 0.121
358
CHL123 Chlamydia 58 0.121
359
P PLY014 Polycystic Kidney Disease 71 0.121
360
TTH006 Tooth Disease 51 0.121
361
P ART021 Arteriosclerosis 53 0.121
362
ACR007 Acromegaly 70 0.121
363
MTR007 Motor Peripheral Neuropathy 41 0.121
364
P FBR017 Fibrosarcoma 55 0.121
365
SQM006 Squamous Cell Carcinoma 59 0.121
366
P HRM001 Hermansky-Pudlak Syndrome 65 0.121
367
P PRP019 Peripheral Nervous System Disease 57 0.121
368
URN010 Urinary Tract Obstruction 55 0.121
369
ESP023 Esophageal Disease 52 0.121
370
IRN002 Iron Metabolism Disease 56 0.121
371
P PLY011 Polycystic Ovary Syndrome 57 0.121
372
NNL005 Non-Alcoholic Fatty Liver Disease 63 0.121
373
ACT098 Acute Erythroid Leukemia 55 0.121
374
P URN019 Urinary Tract Infection 48 0.121
375
c ESS001 Essential Tremor 56 0.121
376
MTH009 Mouth Disease 57 0.121
377
DFF012 Differentiating Neuroblastoma 27 0.121
378
P ART023 Arthropathy 59 0.121
379
LYS002 Lysosomal Storage Disease 51 0.121
380
ALC005 Alcoholic Pancreatitis 38 0.121
381
P PNC044 Pancreatitis 61 0.121
382
P CHR071 Charcot-Marie-Tooth Disease 64 0.121
383
HYD002 Hydronephrosis 58 0.121
384
DNG003 Dengue Disease 65 0.121
385
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.121
386
ANT024 Anthrax Disease 57 0.121
387
DCB001 Decubitus Ulcer 61 0.121
388
c PRG011 Progressive Myoclonus Epilepsy 41 0.121
389
P NRP001 Neuropathy 59 0.121
390
47X002 47,xyy 47 0.121
391
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 41 0.121
392
WLL004 Wallerian Degeneration 38 0.121
393
CLF056 Cleft Lip with or Without Cleft Palate 43 0.121
394
ACT167 Acute Generalized Exanthematous Pustulosis 38 0.121
395
c HRD173 Hereditary Late-Onset Parkinson Disease 50 0.121
396
ERY066 Erythema Multiforme Major 29 0.121
397
c DNT047 Dentinogenesis Imperfecta Type 2 35 0.121
398
P MYC026 Myoclonus Epilepsy 35 0.121
399
P MYC033 Myoclonus 46 0.121
400
P TRM003 Tremor 50 0.121
401
CLF004 Cleft Lip/palate 56 0.121
402
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 31 0.121
403
CRD137 Cardiogenic Shock 56 0.121
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