Search results for ngf

436 hits were found for ngf

# Family MCID Name MIFTS Score
1
c NRP037 Neuropathy, Hereditary Sensory and Autonomic, Type V 56 3.713
2
P NRP001 Neuropathy 56 2.922
3
ATN004 Autonomic Neuropathy 44 2.744
4
P PHC003 Pheochromocytoma 71 2.712
5
P BRS047 Breast Cancer 96 2.710
6
P ALZ034 Alzheimer Disease 88 2.497
7
ALL003 Allergic Rhinitis 67 2.375
8
P CYS018 Cystitis 59 2.202
9
P HNT016 Huntington Disease 71 2.171
10
P MLT020 Multiple Sclerosis 72 2.148
11
P DMN002 Dementia 67 2.148
12
P PSR002 Psoriasis 62 2.136
13
P NRB001 Neuroblastoma 71 2.133
14
ANH002 Anhidrosis 46 2.123
15
P MDL005 Medulloblastoma 77 2.108
16
P MJR001 Major Depressive Disorder 68 2.108
17
ALC007 Alcohol Dependence 66 2.108
18
P CRN028 Corneal Ulcer 47 2.093
19
AST005 Asthma 77 2.076
20
ADN011 Adenoid Cystic Carcinoma 70 2.056
21
CRT072 Creutzfeldt-Jakob Disease 69 2.056
22
P RHN004 Rhinitis 57 2.056
23
P OVR049 Ovarian Disease 53 2.056
24
DBT010 Diabetic Neuropathy 55 1.893
25
ADR040 Adrenal Gland Pheochromocytoma 46 1.885
26
OCL052 Ocular Dominance 41 1.806
27
P DRM053 Dermatitis, Atopic 66 1.794
28
P CHR071 Charcot-Marie-Tooth Disease 64 1.794
29
P PLY019 Polyneuropathy 56 1.782
30
P RTN016 Retinal Degeneration 53 1.782
31
P HRD021 Hereditary Sensory Neuropathy 47 1.782
32
LWC001 Low Compliance Bladder 42 1.782
33
DBT002 Diabetic Autonomic Neuropathy 41 1.782
34
P INT143 Interstitial Cystitis 61 1.768
35
P BPL003 Bipolar Disorder 56 1.754
36
DBT004 Diabetic Polyneuropathy 50 1.754
37
P PRK057 Parkinson Disease, Late-Onset 76 1.739
38
ANX010 Anxiety 72 1.739
39
P ATT013 Attention Deficit-Hyperactivity Disorder 64 1.739
40
IRR002 Irritable Bowel Syndrome 63 1.739
41
SNS003 Sensory Peripheral Neuropathy 53 1.739
42
DMY004 Demyelinating Disease 52 1.739
43
NRM004 Neuroma 51 1.739
44
c AMY091 Amyotrophic Lateral Sclerosis 1 89 1.722
45
P RTT002 Rett Syndrome 80 1.722
46
P SCH015 Schizophrenia 75 1.722
47
c MCR129 Microvascular Complications of Diabetes 1 66 1.722
48
P CRN024 Corneal Disease 43 1.722
49
c HYP595 Hypertension, Essential 84 1.702
50
P CNR004 Cone-Rod Dystrophy 2 71 1.702
51
c NRP053 Neuropathy, Hereditary Sensory and Autonomic, Type Iia 66 1.702
52
P HYD006 Hydrocephalus 65 1.702
53
P SNS001 Sensorineural Hearing Loss 61 1.702
54
FBR047 Fibromyalgia 59 1.702
55
VSC002 Vascular Dementia 57 1.702
56
ADN027 Adenomyosis 57 1.702
57
RLP002 Relapsing-Remitting Multiple Sclerosis 55 1.702
58
KRT006 Keratoconjunctivitis 53 1.702
59
MYL020 Myelomeningocele 51 1.702
60
CCT002 Cicatricial Pemphigoid 50 1.702
61
KRT001 Keratoconjunctivitis Sicca 50 1.702
62
DRY001 Dry Eye Syndrome 47 1.702
63
c CHR087 Chronic Cystitis 35 1.702
64
LSN001 Lesion of Sciatic Nerve 26 1.702
65
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 89 1.679
66
P ATS364 Autism 65 1.679
67
PTT048 Pituitary Adenoma, Prolactin-Secreting 64 1.679
68
LSC001 Lesch-Nyhan Syndrome 62 1.679
69
P CHR654 Charcot-Marie-Tooth Disease, Axonal, Type 2e 61 1.679
70
P NRM002 Normal Pressure Hydrocephalus 56 1.679
71
c SCN036 Secondary Progressive Multiple Sclerosis 55 1.679
72
c CNT035 Central Nervous System Disease 54 1.679
73
P TRT010 Teratoma 51 1.679
74
OPT003 Opiate Dependence 50 1.679
75
BRN009 Burning Mouth Syndrome 49 1.679
76
MNN009 Meningoencephalitis 49 1.679
77
P ASP001 Asperger Syndrome 48 1.679
78
CCN002 Cocaine Abuse 48 1.679
79
SPC010 Speech and Communication Disorders 47 1.679
80
P EPN001 Ependymoblastoma 45 1.679
81
CNN002 Cannabis Abuse 44 1.679
82
P DMY001 Demyelinating Polyneuropathy 41 1.679
83
URT004 Urethral Syndrome 38 1.679
84
ASK001 Askin's Tumor 36 1.679
85
CGH001 Cough Variant Asthma 35 1.679
86
P PRP019 Peripheral Nervous System Disease 57 1.396
87
c PNS012 Paine Syndrome 61 1.344
88
P RTN008 Retinitis Pigmentosa 77 1.320
89
c MGR028 Migraine with or Without Aura 1 69 1.260
90
NRG002 Neurogenic Bladder 54 1.260
91
c NRP054 Neuropathy, Hereditary Sensory and Autonomic, Type Iii 66 1.240
92
EYD002 Eye Disease 58 1.217
93
OCL020 Ocular Cicatricial Pemphigoid 54 1.217
94
PNG002 Pain Agnosia 51 1.217
95
MNN017 Mononeuropathy 39 1.217
96
NRV013 Nerve Growth Factor, Alpha Subunit 8 1.217
97
KRT019 Keratitis, Hereditary 67 1.187
98
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 1.187
99
P NRV007 Nervous System Disease 66 1.187
100
DCB001 Decubitus Ulcer 60 1.187
101
P PRV006 Pervasive Developmental Disorder 57 1.187
102
DSS008 Disease of Mental Health 57 1.187
103
P AGN002 Agnosia 54 1.187
104
CHR100 Chronic Ulcer of Skin 53 1.187
105
P ATN002 Autonomic Nervous System Disease 52 1.187
106
TXC002 Toxic Encephalopathy 52 1.187
107
MSC190 Muscular Disease 51 1.187
108
SMT006 Somatoform Disorder 51 1.187
109
WRN002 Wernicke-Korsakoff Syndrome 49 1.187
110
c NRP044 Neuropathy, Hereditary Sensory and Autonomic, Type Viii 44 1.187
111
P PRP021 Peripheral Nervous System Neoplasm 39 1.187
112
ALG001 Algoneurodystrophy 39 1.187
113
MCC013 Mucocutaneous Ulceration, Chronic 39 1.187
114
c CTR183 Cataract 38 39 1.187
115
NRV004 Nerve Compression Syndrome 38 1.187
116
NRG003 Neurogenic Arthropathy 37 1.187
117
TRG003 Trigeminal Nerve Disease 36 1.187
118
PRR013 Prurigo Nodularis 36 1.187
119
DBT081 Diabetic Encephalopathy 36 1.187
120
DTR001 Detrusor Sphincter Dyssynergia 36 1.187
121
PLY021 Polyradiculopathy 34 1.187
122
SWT003 Sweat Gland Disease 33 1.187
123
SPC003 Specific Developmental Disorder 30 1.187
124
c ATM007 Autoimmune Disease of Central Nervous System 30 1.187
125
PNC012 Punctate Epithelial Keratoconjunctivitis 30 1.187
126
CHL057 Childhood Brain Stem Glioma 29 1.187
127
LMB001 Lumbosacral Plexus Lesion 29 1.187
128
URT023 Ureteric Orifice Cancer 27 1.187
129
P ATN003 Autonomic Nervous System Neoplasm 27 1.187
130
END036 Endocrine Organ Benign Neoplasm 27 1.187
131
NRS001 Neuroschistosomiasis 26 1.187
132
SPR019 Superficial Keratitis 23 1.187
133
MNN015 Mononeuritis of Lower Limb 20 1.187
134
SPN186 Spinal Cord Injury 60 0.178
135
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.149
136
P CHR345 Chronic Pain 50 0.145
137
ALL026 Allergic Hypersensitivity Disease 64 0.140
138
P GLM045 Glioma 63 0.136
139
OST012 Osteoarthritis 78 0.131
140
GLL048 Glial Tumor 45 0.126
141
ISC004 Ischemia 60 0.120
142
ALL014 Allergic Encephalomyelitis 39 0.120
143
DWN001 Down Syndrome 70 0.109
144
c EPS039 Episodic Pain Syndrome, Familial, 1 40 0.109
145
P HRP006 Herpes Simplex 65 0.103
146
CHL014 Cholera 55 0.103
147
TRM010 Traumatic Brain Injury 53 0.103
148
BRN071 Brain Injury 49 0.103
149
DRM006 Dermatitis 61 0.096
150
NRL005 Neurilemmoma 60 0.096
151
RTN023 Retinitis 46 0.096
152
CRB004 Cerebral Artery Occlusion 44 0.096
153
NRR001 Neuroretinitis 43 0.096
154
INS023 Insensitivity to Pain, Congenital, with Anhidrosis 54 0.089
155
NRT004 Neuritis 53 0.089
156
CHR687 Charcot-Marie-Tooth Disease/hereditary Motor and Sensory Neuropathy 40 0.089
157
P PRS040 Prostate Cancer 97 0.081
158
GLB015 Glioblastoma Multiforme 75 0.081
159
P MCR115 Microvascular Complications of Diabetes 5 66 0.081
160
HYP066 Hyperglycemia 61 0.081
161
PST011 Pustulosis of Palm and Sole 52 0.081
162
c PCH010 Pachyonychia Congenita 3 43 0.081
163
PNS018 Pain Sensitivity Quantitative Trait Locus 1 23 0.081
164
P LKM002 Leukemia 66 0.072
165
PRT037 Pertussis 65 0.072
166
DPR016 Depression 63 0.072
167
P END044 Endometriosis 62 0.072
168
MDD011 Mood Disorder 62 0.072
169
ATM095 Autoimmune Disease 61 0.072
170
P BCL017 B-Cell Lymphoma 58 0.072
171
MNT002 Mental Depression 57 0.072
172
AMN003 Amnestic Disorder 54 0.072
173
P SPN052 Spondyloarthropathy 54 0.072
174
SPN119 Spondylarthropathy 44 0.072
175
c MJR024 Major Affective Disorder 9 41 0.072
176
WLL004 Wallerian Degeneration 39 0.072
177
c MJR022 Major Affective Disorder 8 38 0.072
178
CHR178 Chromosomal Triplication 35 0.072
179
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.072
180
P RTN024 Retinoblastoma 72 0.063
181
P TBR001 Tuberous Sclerosis 70 0.063
182
P MSC005 Muscular Dystrophy 66 0.063
183
HYP056 Hypoglycemia 66 0.063
184
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.063
185
MSC007 Muscle Hypertrophy 63 0.063
186
P CTR002 Cataract 60 0.063
187
P SZR006 Seizure Disorder 58 0.063
188
VSL002 Visual Epilepsy 58 0.063
189
P BNC003 Bone Cancer 57 0.063
190
PRS047 Prostatitis 56 0.063
191
P CRD246 Cardiovascular System Disease 56 0.063
192
P FTL001 Fetal Alcohol Syndrome 55 0.063
193
MMM001 Mammary Paget's Disease 53 0.063
194
OCL006 Ocular Hypertension 53 0.063
195
c FML008 Familial Retinoblastoma 53 0.063
196
P THY032 Thyroiditis 53 0.063
197
P AST007 Astrocytoma 50 0.063
198
CYT002 Cytokine Deficiency 44 0.063
199
c PRM038 Primary Agammaglobulinemia 43 0.063
200
P DYS021 Dysautonomia 39 0.063
201
48X005 48,xyyy 39 0.063
202
NRX001 Neuroaxonal Dystrophy 34 0.063
203
P CLR023 Colorectal Cancer 98 0.051
204
P OVR042 Ovarian Cancer 89 0.051
205
c SYS001 Systemic Lupus Erythematosus 86 0.051
207
P GLM040 Glioma Susceptibility 1 81 0.051
208
INS024 Insulin-Like Growth Factor I 79 0.051
209
c TBR025 Tuberous Sclerosis 1 76 0.051
210
P HRT032 Heart Disease 75 0.051
211
SVR004 Severe Combined Immunodeficiency 73 0.051
212
P FML011 Familial Adenomatous Polyposis 72 0.051
213
MSC157 Muscular Dystrophy, Duchenne Type 71 0.051
214
HMN044 Human Immunodeficiency Virus Type 1 71 0.051
215
P AMY004 Amyloidosis 70 0.051
216
CRB039 Cerebrovascular Disease 69 0.051
217
MLN008 Melanoma 69 0.051
218
P HYP086 Hypothyroidism 68 0.051
219
P PLM037 Pulmonary Hypertension 68 0.051
220
P MYS003 Myasthenia Gravis 68 0.051
221
OST159 Osteogenic Sarcoma 66 0.051
222
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 66 0.051
223
P CNJ013 Conjunctivitis 65 0.051
224
P THY023 Thymoma 65 0.051
225
P MTR014 Motor Neuron Disease 64 0.051
226
P SPN046 Spinal Muscular Atrophy 64 0.051
227
P VSC007 Vascular Disease 63 0.051
228
NRF026 Neurofibromatosis, Type Iv, of Riccardi 63 0.051
229
LVR012 Liver Cirrhosis 63 0.051
230
ANR007 Anorexia Nervosa 63 0.051
231
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.051
232
P RHB003 Rhabdomyosarcoma 62 0.051
233
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.051
234
HSH003 Hashimoto Thyroiditis 62 0.051
235
WLL001 Williams-Beuren Syndrome 62 0.051
236
c WLM018 Wilms Tumor 5 62 0.051
237
P LPS004 Lupus Erythematosus 61 0.051
238
OST003 Osteonecrosis 61 0.051
239
SPP011 Suppression of Tumorigenicity 12 59 0.051
240
THY022 Thymic Carcinoma 57 0.051
241
BLM002 Bulimia Nervosa 57 0.051
242
P INF032 Infertility 57 0.051
243
OBS525 Obsolete: Squamous Cell Carcinoma of Head and Neck 57 0.051
244
HYP266 Hypoxia 56 0.051
245
P PLY011 Polycystic Ovary Syndrome 56 0.051
246
GST050 Gastrointestinal System Disease 56 0.051
247
ALL006 Allergic Asthma 56 0.051
248
PRP016 Paraplegia 53 0.051
249
P LTR001 Lateral Sclerosis 53 0.051
250
GNG002 Ganglioneuroma 53 0.051
251
PRS045 Prostatic Hypertrophy 52 0.051
252
IMP005 Impotence 52 0.051
253
P MSC003 Muscular Atrophy 52 0.051
254
OCL069 Ocular Motor Apraxia 51 0.051
255
c VRL010 Viral Hepatitis 51 0.051
256
PRS021 Prostatic Adenoma 51 0.051
257
P TMP001 Temporal Lobe Epilepsy 50 0.051
258
PRS129 Prostatic Hyperplasia, Benign 49 0.051
259
VCC001 Vaccinia 49 0.051
260
BNR002 Bone Resorption Disease 48 0.051
261
P MRC003 Mercury Poisoning 48 0.051
262
HLX001 Helix Syndrome 47 0.051
263
c CHR646 Charcot-Marie-Tooth Disease, Axonal, Type 2b 47 0.051
264
KRT008 Keratopathy 46 0.051
265
HYP457 Hypertrophic Scars 43 0.051
266
BCK006 Back Pain 42 0.051
267
ANX004 Anoxia 42 0.051
268
FML307 Familial Calcium Pyrophosphate Deposition 38 0.051
269
OVR094 Ovarian Epithelial Cancer 38 0.051
270
NRT011 Neurotrophic Keratopathy 36 0.051
271
HRW001 Hair Whorl 36 0.051
273
PLY150 Polykaryocytosis Inducer 31 0.051
274
P HPT023 Hepatocellular Carcinoma 100 0.036
275
P PNC035 Pancreatic Cancer 84 0.036
276
P GST053 Gastric Cancer 83 0.036
277
P RHM011 Rheumatoid Arthritis 80 0.036
278
c MNN043 Meningioma, Familial 74 0.036
279
BRN028 Brain Cancer 73 0.036
280
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.036
281
LPT014 Leptin Deficiency or Dysfunction 73 0.036
282
c HYP836 Hypercholesterolemia, Familial, 1 72 0.036
283
c NRF024 Neurofibromatosis, Type I 71 0.036
284
PRP027 Peripheral Vascular Disease 71 0.036
285
P WSK001 Wiskott-Aldrich Syndrome 71 0.036
286
P ART022 Arthritis 70 0.036
287
CNG034 Congestive Heart Failure 70 0.036
288
ADL002 Adult Syndrome 69 0.036
289
RCK004 Rickets 69 0.036
290
P FRG001 Fragile X Syndrome 68 0.036
291
P SPR120 Supranuclear Palsy, Progressive, 1 68 0.036
292
c PRM196 Premature Ovarian Failure 1 68 0.036
293
EWN003 Ewing Sarcoma 68 0.036
294
SKN019 Skin Melanoma 67 0.036
295
c ATS007 Autism Spectrum Disorder 67 0.036
296
P CRD119 Cardiac Arrest 67 0.036
297
THY111 Thyroid Carcinoma, Familial Medullary 67 0.036
298
P SKN015 Skin Carcinoma 67 0.036
299
CNN005 Connective Tissue Disease 66 0.036
300
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.036
301
P ATR011 Atrial Fibrillation 66 0.036
302
MRK001 Merkel Cell Carcinoma 66 0.036
303
CHG001 Chagas Disease 66 0.036
304
ATH013 Atherosclerosis Susceptibility 66 0.036
305
SRC014 Sarcoma 65 0.036
306
c RHB024 Rhabdomyosarcoma 2 65 0.036
307
P TRN020 Turner Syndrome 65 0.036
308
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.036
309
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 65 0.036
310
INC002 Inclusion Body Myositis 64 0.036
311
P DBT009 Diabetes Mellitus 64 0.036
312
P MYP004 Myopathy 64 0.036
313
NRF007 Neurofibroma 64 0.036
314
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.036
315
TTN003 Tetanus 64 0.036
316
KHL003 Kohlschutter-Tonz Syndrome 64 0.036
317
c PRC016 Pre-Eclampsia 63 0.036
318
P MST009 Mastocytosis 63 0.036
319
c SCL052 Scleroderma, Familial Progressive 62 0.036
320
P PRD008 Periodontitis 62 0.036
321
BRS099 Breast Ductal Carcinoma 62 0.036
322
CLT003 Colitis 62 0.036
323
TRN015 Transient Cerebral Ischemia 62 0.036
324
BLL006 Bullous Pemphigoid 62 0.036
325
PSR001 Psoriatic Arthritis 62 0.036
326
NTR005 Nutritional Deficiency Disease 61 0.036
327
c BRN108 Branchiootic Syndrome 1 61 0.036
328
P ENC018 Encephalopathy 61 0.036
329
VRL011 Viral Infectious Disease 61 0.036
330
PHL006 Phelan-Mcdermid Syndrome 61 0.036
331
CNG410 Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly 60 0.036
332
RTN017 Retinal Detachment 60 0.036
333
INS001 Insulinoma 60 0.036
334
SQM006 Squamous Cell Carcinoma 60 0.036
335
WST001 West Syndrome 60 0.036
336
ETN001 Eating Disorder 59 0.036
337
P GLL022 Guillain-Barre Syndrome 59 0.036
338
P MYC008 Myocarditis 59 0.036
339
THY029 Thyroid Carcinoma 59 0.036
340
STT001 Status Epilepticus 59 0.036
341
SPN027 Spinal Stenosis 59 0.036
342
HLC007 Helicobacter Pylori Infection 59 0.036
343
ADN018 Adenoma 58 0.036
344
CMP010 Complex Regional Pain Syndrome 58 0.036
345
PST028 Post-Traumatic Stress Disorder 58 0.036
346
c ACT073 Acute Leukemia 58 0.036
347
ERY029 Erythermalgia, Primary 58 0.036
348
P URT039 Urticaria 58 0.036
349
P OPT006 Optic Nerve Disease 57 0.036
350
EMB004 Embryonal Carcinoma 57 0.036
351
P SJG008 Sjogren Syndrome 56 0.036
352
P STR020 Strabismus 56 0.036
353
SPN041 Spinal Cord Disease 56 0.036
354
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.036
355
P FBR017 Fibrosarcoma 56 0.036
356
AGN016 Aging 56 0.036
357
c CHR627 Charcot-Marie-Tooth Disease, Demyelinating, Type 1a 56 0.036
358
P MLN007 Male Infertility 56 0.036
359
P MYS005 Myositis 56 0.036
360
SYN007 Synovitis 55 0.036
361
GNG005 Gangliocytoma 55 0.036
362
P HYP076 Hyperthyroidism 55 0.036
363
CLF004 Cleft Lip/palate 54 0.036
364
P GNR002 Generalized Epilepsy with Febrile Seizures Plus 54 0.036
365
GNT003 Genital Herpes 54 0.036
366
c OPT053 Optic Atrophy 1 54 0.036
367
P TCD001 Tic Disorder 54 0.036
368
GST023 Gastric Ulcer 53 0.036
369
CLF001 Cleft Lip 53 0.036
370
P RTN018 Retinal Disease 52 0.036
371
c MCR113 Microvascular Complications of Diabetes 3 52 0.036
372
P SML001 Small Cell Carcinoma 52 0.036
373
CHR073 Choreatic Disease 52 0.036
374
ANK001 Ankylosis 52 0.036
375
NRL002 Neurilemmomatosis 51 0.036
376
THY125 Thyroid Gland Medullary Carcinoma 51 0.036
377
SPN035 Spindle Cell Sarcoma 51 0.036
378
RTN003 Retinal Ischemia 50 0.036
379
DYS073 Dysphagia 50 0.036
380
ALL009 Allergic Conjunctivitis 50 0.036
381
P OVR082 Overgrowth Syndrome 50 0.036
382
VRC001 Varicocele 49 0.036
383
LRN003 Learning Disability 49 0.036
384
47X002 47,xyy 49 0.036
385
SKN013 Skin Benign Neoplasm 49 0.036
386
VTM002 Vitamin B12 Deficiency 48 0.036
387
ATS010 Autosomal Recessive Disease 48 0.036
388
ACT084 Acute Stress Disorder 48 0.036
389
c MCR120 Microvascular Complications of Diabetes 7 47 0.036
390
ATN005 Autonomic Dysfunction 47 0.036
391
TTH006 Tooth Disease 46 0.036
392
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 46 0.036
393
LMB050 Limbal Stem Cell Deficiency 45 0.036
394
HDN002 Head Injury 45 0.036
395
c MLG068 Malignant Glioma 45 0.036
396
RTR008 Root Resorption 45 0.036
397
ASP004 Asphyxia Neonatorum 45 0.036
398
HRN003 Heroin Dependence 44 0.036
399
CRT015 Carotid Artery Occlusion 44 0.036
400
CHD004 Chudley-Mccullough Syndrome 44 0.036
401
PRS042 Prostate Disease 44 0.036
402
HPT004 Hepatic Coma 43 0.036
403
P CLS010 Cluster Headache 43 0.036
404
c FTL006 Fetal Alcohol Spectrum Disorder 42 0.036
405
BNS007 Bone Sarcoma 42 0.036
406
MYF002 Myofascial Pain Syndrome 42 0.036
407
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 42 0.036
408
TND006 Tendinosis 42 0.036
409
c MCR130 Microvascular Complications of Diabetes 6 41 0.036
410
c MCR133 Microvascular Complications of Diabetes 4 41 0.036
411
SPN369 Spinal Disease 41 0.036
412
END011 Endometriosis of Ovary 40 0.036
413
PRM329 Premature Aging 39 0.036
414
MCH006 Mechanical Strabismus 39 0.036
415
HMR023 Hemorrhagic Cystitis 38 0.036
416
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.036
417
MST004 Mast Cell Neoplasm 38 0.036
418
EXT007 Extracutaneous Mastocytoma 38 0.036
419
P SCH077 Schwannomatosis 1 38 0.036
420
FST001 Foster-Kennedy Syndrome 37 0.036
421
c ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 36 0.036
423
RRS014 Rare Surgical Neurologic Disease 32 0.036
424
PRL014 Paralytic Squint 29 0.036
425
TBL029 Tubulin, Beta 28 0.036
426
SCT001 Sciatic Neuropathy 28 0.036
427
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 28 0.036
428
RRD056 Rare Disease in Surgical Orthopedic 28 0.036
429
P FML340 Familial Episodic Pain Syndrome 27 0.036
430
c CRN110 Cranioectodermal Dysplasia 3 27 0.036
431
NRL008 Neural Crest Tumor 27 0.036
432
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.036
433
NRP027 Neuropathy, Painful 24 0.036
434
HYP144 Hyperacusis 23 0.036
435
P ANT080 Antigen Defined by Monoclonal Antibody Aj9 18 0.036
436
MYL068 Myelinated Optic Nerve Fibers 11 0.036
Content
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