Search results for amh

560 hits were found for amh

# Family MCID Name MIFTS Score
1
PRS128 Persistent Mullerian Duct Syndrome, Types I and Ii 43 36.068
2
P PRS049 Persistent Mullerian Duct Syndrome 51 35.649
3
P PLY011 Polycystic Ovary Syndrome 57 24.353
4
P INF032 Infertility 60 20.826
5
P HYP730 Hypogonadotropic Hypogonadism 57 15.206
6
OVR029 Ovarian Hyperstimulation Syndrome 63 14.067
7
PRM013 Premature Menopause 57 13.633
8
CRY035 Cryptorchidism, Unilateral or Bilateral 57 13.353
9
P GND004 Gonadal Dysgenesis 46 12.567
10
P OVR049 Ovarian Disease 50 12.268
11
P TRN020 Turner Syndrome 67 11.061
12
ANV001 Anovulation 46 11.007
13
VRC001 Varicocele 48 10.778
14
PSD009 Pseudohermaphroditism 46 10.750
15
MCC012 Mccune-Albright Syndrome 69 10.381
16
P TRT010 Teratoma 50 10.268
17
MYM001 Myoma 54 9.977
18
P OVR046 Ovarian Cyst 43 9.835
19
P GLC113 Galactosemia I 65 9.491
20
c BNG093 Benign Teratoma 39 9.339
21
P MXD016 Mixed Gonadal Dysgenesis 34 9.142
22
ING001 Inguinal Hernia 59 8.640
23
P DSR090 Disorder of Sexual Development 45 8.322
24
DSS008 Disease of Mental Health 74 8.239
25
AND002 Androgen Insensitivity Syndrome 63 8.063
26
END011 Endometriosis of Ovary 40 7.781
27
HRM002 Hermaphroditism 35 7.761
28
P KLL001 Kallmann Syndrome 65 7.571
29
FRM001 Freemartinism 17 7.348
30
P CMP005 Campomelic Dysplasia 65 7.260
31
TST015 Testicular Disease 42 6.958
32
OLG001 Oligospermia 45 6.948
33
OLG022 Oligoasthenoteratozoospermia 36 6.882
34
P INH011 Inherited Bone Marrow Failure Syndromes 33 6.794
35
GND001 Gonadoblastoma 42 6.735
36
MLL011 Mullerian Aplasia and Hyperandrogenism 45 6.522
37
PST113 Posterior Fossa Ependymoma 28 6.522
38
c 46X082 46,xy Sex Reversal 52 6.522
39
TST044 Testicular Torsion 45 6.486
40
P SLP003 Salpingitis 39 6.486
41
P RNL100 Renal Hypodysplasia/aplasia 1 63 6.439
42
P SLP004 Salpingo-Oophoritis 23 6.439
43
c 46X081 46,xx Sex Reversal 34 6.439
44
c CHR018 Chronic Salpingo-Oophoritis 22 6.439
45
UTR031 Uterine Benign Neoplasm 30 6.325
46
OVR041 Ovarian Benign Neoplasm 32 6.325
47
NSP004 Nosophobia 24 6.325
48
RPR001 Reproductive Organ Benign Neoplasm 31 6.325
49
MXL016 Maxillonasal Dysplasia, Binder Type 32 6.325
50
45X001 45,x/46,xy Mixed Gonadal Dysgenesis 33 6.325
51
SBS001 Subserous Uterine Fibroid 24 6.325
52
STR018 Steroid Inherited Metabolic Disorder 33 6.325
53
c 46X030 46,xy Sex Reversal 9 43 6.325
54
SLP002 Salpingitis Isthmica Nodosa 26 6.325
55
c BNG029 Benign Struma Ovarii 34 6.325
56
OVR057 Ovarian Serous Adenofibroma 29 6.325
57
DRM005 Dermoid Cyst of Ovary 29 6.325
58
CNC001 Cancerophobia 27 6.325
59
ADH001 Adhesions of Uterus 31 6.325
60
OVR005 Ovarian Large-Cell Neuroendocrine Carcinoma 29 6.325
61
PST029 Postmenopausal Atrophic Vaginitis 39 6.325
62
TST005 Testicular Gonadoblastoma 22 6.325
63
OVR002 Ovarian Serous Cystadenofibroma 29 6.325
64
INH003 Inhibited Female Orgasm 29 6.325
65
SBC017 Sebaceous Gland Disease 42 6.325
66
PLV004 Pelvic Varices 35 6.325
67
HMM001 Hemometra 27 6.325
68
P END044 Endometriosis 62 5.639
69
HYP043 Hyperandrogenism 47 5.620
70
HYP080 Hypogonadism 49 5.312
71
AMN001 Amenorrhea 53 4.236
72
AGN016 Aging 53 3.478
73
AZS001 Azoospermia 45 2.833
74
ANR018 Anorchia 36 2.543
75
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 2.526
76
P BRS047 Breast Cancer 97 2.522
77
P PRC019 Precocious Puberty 48 2.406
78
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 2.216
79
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 2.216
80
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 2.216
81
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 2.216
82
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 2.216
83
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 2.216
84
c BDY019 Body Mass Index Quantitative Trait Locus 18 46 2.216
85
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 2.216
86
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 2.216
87
P BDY004 Body Mass Index Quantitative Trait Locus 11 82 2.171
88
P OVR042 Ovarian Cancer 88 2.148
89
47X002 47,xyy 47 2.097
90
CNG562 Congenital Hypogonadotropic Hypogonadism 28 1.978
91
c CNT075 Central Precocious Puberty 53 1.905
92
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 1.896
93
DWN001 Down Syndrome 70 1.892
94
c PRC016 Pre-Eclampsia 64 1.871
95
P VSC007 Vascular Disease 62 1.744
96
MBS002 Moebius Syndrome 53 1.716
97
P ACN011 Acne 55 1.703
98
RCK004 Rickets 64 1.685
99
LPD012 Lipoid Congenital Adrenal Hyperplasia 68 1.652
100
ART002 Arts Syndrome 66 1.629
101
P HYP535 Hypogonadotropic Hypogonadism 7 with or Without Anosmia 57 1.539
102
ECT026 Ectopic Pregnancy 47 1.501
103
LMY002 Leiomyoma 51 1.479
104
P HYP086 Hypothyroidism 68 1.471
105
HYP060 Hyperinsulinism 53 1.463
106
P HYP040 Hypospadias 51 1.463
107
CMP034 Complete Androgen Insensitivity Syndrome 55 1.448
108
ISL004 Isolated Gonadotropin-Releasing Hormone Deficiency 27 1.446
109
HYP784 Hypogonadism, Male 43 1.440
110
THY029 Thyroid Carcinoma 55 1.440
111
MYF001 Myofibroma 42 1.426
112
PPL052 Papillomatosis, Confluent and Reticulated 34 1.424
113
c 46X055 46,xy Sex Reversal 3 40 1.424
114
c TYP008 Type 1 Diabetes Mellitus 77 1.400
115
P MYR002 Mayer-Rokitansky-Kuster-Hauser Syndrome 59 1.375
116
P SYN140 Syndrome with 46,xy Disorder of Sex Development 23 1.362
117
CHR178 Chromosomal Triplication 33 1.358
118
48X005 48,xyyy 39 1.323
119
c WLM013 Wilms Tumor 1 65 1.314
120
c ART138 Aortic Aneurysm, Familial Abdominal, 1 60 1.292
121
ART016 Aortic Aneurysm 68 1.292
122
P VND001 Vein Disease 42 1.292
123
P DBT009 Diabetes Mellitus 67 1.285
124
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 1.225
125
PLY105 Polycystic Ovary Syndrome 1 39 1.213
126
TST014 Testicular Cancer 51 1.170
127
PNS014 Penis Agenesis 38 1.158
128
ATS010 Autosomal Recessive Disease 42 1.146
129
P ATT013 Attention Deficit-Hyperactivity Disorder 65 1.146
130
ETN001 Eating Disorder 59 1.146
131
ADN027 Adenomyosis 59 1.139
132
P SPR119 Spermatogenic Failure, X-Linked, 1 36 1.134
133
P ALP008 Alopecia 53 1.121
134
c SYS001 Systemic Lupus Erythematosus 85 1.113
135
P LPS004 Lupus Erythematosus 61 1.113
136
HYP056 Hypoglycemia 65 1.082
137
DFC004 Deficiency Anemia 74 1.068
138
LPD008 Lipid Metabolism Disorder 61 1.068
139
P OCY003 Oocyte Maturation Defect 1 46 1.051
140
ANT039 Antisynthetase Syndrome 55 1.051
141
P FRG001 Fragile X Syndrome 70 1.023
142
P ADN016 Adenocarcinoma 63 1.023
143
P SRC025 Sarcoidosis 1 70 1.007
144
PTZ001 Peutz-Jeghers Syndrome 69 1.007
145
EXT034 Extrinsic Allergic Alveolitis 56 1.007
146
LNG099 Lung Disease 62 1.007
147
LPT014 Leptin Deficiency or Dysfunction 77 0.990
148
P PHC003 Pheochromocytoma 70 0.977
149
ADR040 Adrenal Gland Pheochromocytoma 45 0.977
150
SCK003 Sickle Cell Anemia 74 0.972
151
c SPR162 Spermatogenic Failure 50 42 0.972
152
c BDY021 Body Mass Index Quantitative Trait Locus 20 49 0.971
153
c 46X079 46,xy Sex Reversal 11 41 0.954
154
TST035 Testicular Anomalies with or Without Congenital Heart Disease 20 0.954
155
GLC003 Glucose Intolerance 53 0.954
156
BLR008 Bilirubin Metabolic Disorder 57 0.934
157
P MLN007 Male Infertility 56 0.916
158
DPH001 Diphtheria 59 0.914
159
LMY014 Leiomyoma, Uterine 55 0.907
160
MDD011 Mood Disorder 61 0.891
161
LYM133 Lymphoma, Hodgkin, Classic 69 0.887
162
P RHM011 Rheumatoid Arthritis 81 0.880
163
AND014 Androgenic Alopecia 46 0.867
164
P ALP061 Alopecia, Androgenetic, 1 48 0.867
165
END057 Endometrial Cancer 76 0.865
166
OVR073 Ovarian Remnant Syndrome 14 0.858
167
VGN023 Vaginitis 56 0.858
168
PLY100 Polyploidy 36 0.840
169
P THY032 Thyroiditis 56 0.835
170
P ART022 Arthritis 70 0.827
171
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 0.810
172
c OVR120 Ovarian Dysgenesis 8 19 0.794
173
c 46X048 46,xx Sex Reversal 2 27 0.794
174
c PRM094 Premature Ovarian Failure 5 23 0.794
175
c 46X058 46,xy Sex Reversal 10 23 0.794
176
c PRM295 Premature Ovarian Failure 15 20 0.794
177
GND014 Gonadal Dysgenesis, Dysmorphic Facies, Retinal Dystrophy, and Myopathy 22 0.794
178
RTN191 Retinal Dystrophy with or Without Extraocular Anomalies 19 0.794
179
GST033 Gestational Diabetes 60 0.787
180
CYS001 Cystic Fibrosis 77 0.774
181
P TXP001 Toxoplasmosis 59 0.774
182
OVR094 Ovarian Epithelial Cancer 39 0.771
183
P GLM040 Glioma Susceptibility 1 70 0.748
184
c CHR684 Chronic Kidney Disease 73 0.728
185
ADR049 Adrenal Hypoplasia, Congenital 52 0.727
186
P LYM118 Lymphoma 66 0.700
187
P BLD134 Bladder Cancer 79 0.700
188
HYP020 Hyperprolactinemia 63 0.682
189
P PNC035 Pancreatic Cancer 87 0.664
190
LYM143 Lymphoma, Non-Hodgkin, Familial 74 0.633
191
RPD005 Rapidly Involuting Congenital Hemangioma 48 0.633
192
HMT008 Hematuria, Benign Familial 54 0.607
193
c PNS012 Paine Syndrome 60 0.607
194
ACR041 Acromelic Frontonasal Dysostosis 53 0.607
195
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.607
196
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.607
197
P INT143 Interstitial Cystitis 59 0.607
198
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.607
199
c HYP548 Hypogonadotropic Hypogonadism 2 with or Without Anosmia 37 0.601
200
P NRB001 Neuroblastoma 66 0.601
201
GRN022 Granulosa Cell Tumor of the Ovary 34 0.601
202
P PLV020 Pelvic Organ Prolapse 57 0.590
203
ANR007 Anorexia Nervosa 59 0.590
204
MTR010 Mature Teratoma 40 0.590
205
P CYS017 Cystic Teratoma 41 0.579
206
ADR041 Adrenal Cortical Adenoma 48 0.557
207
ATM095 Autoimmune Disease 61 0.557
208
HMS001 Hemosiderosis 48 0.557
209
P MYL006 Myeloid Leukemia 60 0.557
210
P RRH023 Rare Hereditary Hemochromatosis 52 0.557
211
CRH001 Crohn's Disease 80 0.545
212
P MLT020 Multiple Sclerosis 79 0.533
213
CNN003 Conn's Syndrome 77 0.533
214
CNG410 Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly 60 0.521
215
SCT005 Scott Syndrome 51 0.521
216
END062 Endometrial Hyperplasia 47 0.521
217
ANG033 Angiomyomatous Hamartoma 11 0.521
218
P ECL001 Eclampsia 52 0.508
219
P MLT074 Multiple Endocrine Neoplasia 58 0.508
220
TWN007 Twinning, Dizygotic 21 0.495
221
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.495
222
SVR004 Severe Combined Immunodeficiency 70 0.495
223
ATH013 Atherosclerosis Susceptibility 63 0.482
224
P PRD006 Prader-Willi Syndrome 60 0.482
225
c FNC027 Fanconi Anemia, Complementation Group a 80 0.482
226
HSH003 Hashimoto Thyroiditis 60 0.482
227
P HRD200 Hereditary Breast Ovarian Cancer Syndrome 67 0.482
228
DFF036 Differentiated Thyroid Carcinoma 51 0.482
229
NRM001 Neuromyelitis Optica 60 0.482
230
PRT251 Proteinuria, Chronic Benign 58 0.468
231
P EPL164 Epilepsy 70 0.468
232
P PRS038 Personality Disorder 65 0.468
233
P SZR006 Seizure Disorder 69 0.468
234
THY030 Thyroid Gland Disease 50 0.455
235
c LKM061 Leukemia, Acute Myeloid 83 0.440
236
IMM167 Immune Deficiency Disease 76 0.440
237
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 0.440
238
CYT002 Cytokine Deficiency 43 0.440
239
P LKM062 Leukemia, Acute Lymphoblastic 69 0.425
240
P SCK005 Sickle Cell Disease 56 0.425
241
c SPR086 Spermatogenic Failure 3 47 0.410
242
P LKM002 Leukemia 65 0.410
243
CYS009 Cystadenoma 42 0.410
244
IGG001 Iga Glomerulonephritis 50 0.410
245
c 46X011 46, Xy Disorders of Sexual Development 20 0.410
246
c MLT160 Multiple Endocrine Neoplasia, Type Iia 67 0.394
247
P MYT002 Myotonic Dystrophy 51 0.394
248
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 0.394
249
EST002 Estrogen-Receptor Negative Breast Cancer 45 0.377
250
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 0.377
251
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 58 0.377
252
DMY004 Demyelinating Disease 50 0.377
253
c DWL002 Dowling-Degos Disease 1 58 0.359
254
ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 35 0.359
255
PTT009 Pituitary Gland Disease 52 0.359
256
P SKN015 Skin Carcinoma 71 0.359
257
P CRN300 Coronary Heart Disease 1 73 0.341
258
SXL003 Sexual Disorder 49 0.341
259
c SCL052 Scleroderma, Familial Progressive 60 0.341
260
P FML018 Familial Mediterranean Fever 73 0.341
261
INS024 Insulin-Like Growth Factor I 77 0.341
262
P CLR023 Colorectal Cancer 100 0.341
263
P DYS007 Dyskeratosis Congenita 66 0.341
264
ISC004 Ischemia 61 0.341
265
BRC012 Brucellosis 66 0.341
266
P DMN001 Diamond-Blackfan Anemia 73 0.341
267
PLC005 Placental Insufficiency 55 0.341
268
3BT001 3-Beta-Hydroxysteroid Dehydrogenase Deficiency 40 0.341
269
GRM010 Germ Cells Tumors 33 0.341
270
INF118 Inflammatory Myopathy with Abundant Macrophages 27 0.341
271
NRM018 Normosmic Congenital Hypogonadotropic Hypogonadism 45 0.341
272
c DNT047 Dentinogenesis Imperfecta Type 2 35 0.341
273
P PTS002 Ptosis 52 0.321
274
BLP046 Blepharophimosis, Ptosis, and Epicanthus Inversus 56 0.321
275
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.321
276
P GRF003 Graft-Versus-Host Disease 71 0.321
277
c HYP595 Hypertension, Essential 84 0.321
278
EPC005 Epicanthus 35 0.321
279
BLP004 Blepharophimosis 36 0.321
280
c SVR005 Severe Pre-Eclampsia 49 0.321
281
OST012 Osteoarthritis 77 0.321
282
P THL005 Thalassemia 56 0.321
283
SFT003 Soft Tissue Sarcoma 43 0.321
284
HYP266 Hypoxia 56 0.321
285
P APL001 Aplastic Anemia 72 0.301
286
ANL022 Anal Fistula 47 0.301
287
P CLC063 Celiac Disease 1 65 0.301
288
ANS023 Anus, Imperforate 56 0.301
289
c HYD046 Hydatidiform Mole, Recurrent, 1 59 0.301
290
OST159 Osteogenic Sarcoma 66 0.301
291
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 0.301
292
EWN003 Ewing Sarcoma 69 0.301
293
DNY001 Denys-Drash Syndrome 57 0.301
295
CTN028 Cutaneous Telangiectasia and Cancer Syndrome, Familial 70 0.301
296
P TMR010 Tumor Predisposition Syndrome 69 0.301
297
ACR007 Acromegaly 70 0.301
298
ADN075 Adenomyoma 31 0.301
299
SMN007 Seminoma 42 0.301
300
PDT001 Pediatric Lymphoma 28 0.301
301
SPN035 Spindle Cell Sarcoma 51 0.301
302
GST010 Gestational Trophoblastic Neoplasm 52 0.301
303
c ACT073 Acute Leukemia 59 0.301
304
SRC014 Sarcoma 64 0.301
305
c JVN010 Juvenile Rheumatoid Arthritis 52 0.301
306
END086 End Stage Renal Disease 54 0.301
307
HRD031 Hereditary Paraganglioma-Pheochromocytoma Syndromes 61 0.301
308
ASH001 Asherman's Syndrome 34 0.301
309
INH023 Inherited Cancer-Predisposing Syndrome 53 0.301
310
PST092 Posttransplant Acute Limbic Encephalitis 29 0.301
311
c ATS007 Autism Spectrum Disorder 71 0.278
312
MYL009 Myelodysplastic Syndrome 67 0.278
313
P NNN008 Noonan Syndrome 1 76 0.278
314
c TYP009 Type 2 Diabetes Mellitus 91 0.278
315
LRN002 Laron Syndrome 62 0.278
316
LYM007 Lymphangioleiomyomatosis 68 0.278
317
c TBR025 Tuberous Sclerosis 1 84 0.278
318
GRN037 Granulomatosis with Polyangiitis 66 0.278
319
RNL114 Renal Cell Carcinoma, Nonpapillary 79 0.278
320
PRV003 Perivascular Epithelioid Cell Tumor 38 0.278
321
P TBR001 Tuberous Sclerosis 69 0.278
322
P PRP019 Peripheral Nervous System Disease 57 0.278
323
P ANT006 Antiphospholipid Syndrome 55 0.278
324
P MYP004 Myopathy 67 0.278
325
PST011 Pustulosis of Palm and Sole 52 0.278
326
PSY004 Psychotic Disorder 66 0.278
327
AMP009 Ampulla of Vater Adenocarcinoma 36 0.278
328
MCR013 Microphthalmia 59 0.278
329
AVD001 Avoidant Personality Disorder 49 0.278
330
P PSR002 Psoriasis 63 0.278
331
CRV002 Cervix Uteri Carcinoma in Situ 48 0.278
332
P HYP083 Hypopituitarism 51 0.278
333
P CRN028 Corneal Ulcer 47 0.278
334
P NRP001 Neuropathy 59 0.278
335
DRT002 Duarte Variant Galactosemia 13 0.278
336
ATM023 Autoimmune Oophoritis 16 0.278
337
ALD013 Aldosterone-Producing Adenoma 36 0.278
338
P MSC005 Muscular Dystrophy 66 0.278
339
CRV045 Cervical Intraepithelial Neoplasia 38 0.278
340
FMR019 Fmr1 Disorders 13 0.278
341
TRM010 Traumatic Brain Injury 50 0.278
343
c PSD047 Pseudo-Turner Syndrome 52 0.278
344
BRN071 Brain Injury 50 0.278
345
P PRV006 Pervasive Developmental Disorder 52 0.254
346
P SLV027 Silver-Russell Syndrome 1 52 0.254
347
c PRM196 Premature Ovarian Failure 1 58 0.254
348
PSD021 Pseudovaginal Perineoscrotal Hypospadias 44 0.254
349
DSS032 Disease by Infectious Agent 55 0.254
350
c 46X049 46,xy Sex Reversal 2 51 0.254
351
P MYC084 Mycobacterium Tuberculosis 1 68 0.254
352
HLC007 Helicobacter Pylori Infection 67 0.254
353
PHY002 Physical Disorder 40 0.254
354
CHL123 Chlamydia 58 0.254
355
HST010 Histiocytosis 49 0.254
356
IMP005 Impotence 52 0.254
357
INF021 Infant Gynecomastia 30 0.254
358
P MYP006 Myopia 55 0.254
359
GYN001 Gynecomastia 48 0.254
360
P END039 Endodermal Sinus Tumor 42 0.254
361
SRT002 Sertoli Cell Tumor 38 0.254
362
PLC008 Placenta Disease 48 0.254
363
OVR012 Ovarian Serous Cystadenocarcinoma 55 0.254
364
P INS002 in Situ Carcinoma 52 0.254
365
PTT041 Pituitary Stalk Interruption Syndrome 54 0.254
366
DNC004 Diencephalic Syndrome 36 0.254
367
CLS031 Classic Galactosemia and Clinical Variant Galactosemia 18 0.254
368
NNS011 Nonseminomatous Germ Cell Tumor 32 0.254
369
P CHR345 Chronic Pain 50 0.254
370
PNG002 Pain Agnosia 51 0.227
371
RTN017 Retinal Detachment 60 0.227
372
P ATS364 Autism 72 0.227
373
TKY002 Takayasu Arteritis 61 0.227
374
P FCS012 Facioscapulohumeral Muscular Dystrophy 1 68 0.227
375
MSC157 Muscular Dystrophy, Duchenne Type 78 0.227
376
c SPN225 Spondyloarthropathy 1 70 0.227
377
c MYT020 Myotonic Dystrophy 2 57 0.227
378
OVR112 Ovarian Germ Cell Cancer 41 0.227
379
HMC014 Homocysteinemia 52 0.227
380
P PLM037 Pulmonary Hypertension 69 0.227
381
P UTR058 Uterine Anomalies 47 0.227
382
c BTT014 Beta-Thalassemia 72 0.227
383
ACN002 Acanthosis Nigricans 56 0.227
384
CHL152 Childhood Acute Lymphocytic Leukemia 50 0.227
385
ADN018 Adenoma 58 0.227
386
SPN051 Spondylitis 51 0.227
387
P KDN018 Kidney Disease 71 0.227
388
P HRT032 Heart Disease 84 0.227
389
BTT017 Beta-Thalassemia Major 54 0.227
390
P URN019 Urinary Tract Infection 48 0.227
391
c VRL010 Viral Hepatitis 52 0.227
392
P KDN017 Kidney Cancer 60 0.227
393
EST004 Estrogen Excess 37 0.227
394
INF009 Inflammatory Spondylopathy 30 0.227
395
MCL003 Macular Holes 44 0.227
396
SKN019 Skin Melanoma 70 0.227
397
ACT250 Acute Megakaryocytic Leukemia 63 0.227
398
c CHR417 Chronic Graft Versus Host Disease 55 0.227
399
MYT011 Myotonia 37 0.227
400
BCR002 Bicornuate Uterus 24 0.227
401
P SCH015 Schizophrenia 74 0.197
402
P MDL005 Medulloblastoma 75 0.197
403
NRL016 Neural Tube Defects 80 0.197
404
MLB001 Mulibrey Nanism 51 0.197
405
c MLT156 Multiple Endocrine Neoplasia, Type I 71 0.197
406
AND020 Androgen Insensitivity, Partial 54 0.197
407
PTT046 Pituitary Hormone Deficiency, Combined, 2 62 0.197
408
CHR103 Charge Syndrome 65 0.197
409
GND011 Gonadal Agenesis 20 0.197
410
HRT030 Hartsfield Syndrome 46 0.197
411
ACN029 Acne, Adult 7 0.197
412
CRV035 Cervical Cancer 72 0.197
413
PRS129 Prostatic Hyperplasia, Benign 48 0.197
414
c SCH051 Schizophrenia 4 35 0.197
415
CHL149 Childhood Acute Myeloid Leukemia 42 0.197
416
P PLY041 Polymyositis 58 0.197
417
MLG169 Malignant Astrocytoma 57 0.197
418
P TMP001 Temporal Lobe Epilepsy 49 0.197
419
P HMN010 Hemangioma 61 0.197
420
ANP005 Anaplastic Astrocytoma 59 0.197
421
SQM006 Squamous Cell Carcinoma 59 0.197
422
P BNG030 Benign Ependymoma 51 0.197
423
CLL010 Cellular Ependymoma 58 0.197
424
TST018 Testicular Yolk Sac Tumor 38 0.197
425
NNL005 Non-Alcoholic Fatty Liver Disease 63 0.197
426
ART074 Aortic Dissection 53 0.197
427
GRM005 Germ Cell Cancer 46 0.197
428
PRS021 Prostatic Adenoma 43 0.197
429
VGN019 Vaginal Discharge 33 0.197
430
P SBS003 Substance Abuse 54 0.197
431
PRS045 Prostatic Hypertrophy 53 0.197
432
ACT003 Acute Kidney Tubular Necrosis 46 0.197
433
P TST026 Testicular Germ Cell Cancer 42 0.197
434
LRN003 Learning Disability 49 0.197
435
P BCL017 B-Cell Lymphoma 57 0.197
436
HDG002 Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance 42 0.197
437
FTT001 Fatty Liver Disease 61 0.197
438
P HYP055 Hypoplastic Left Heart Syndrome 65 0.197
439
P HYP076 Hyperthyroidism 53 0.197
440
P HRD086 Hereditary Hypophosphatemic Rickets 40 0.197
441
IDP034 Idiopathic Central Precocious Puberty 27 0.197
442
MXD032 Mixed Germ Cell Tumor 24 0.197
443
c ATS454 Autosomal Trisomy 17 0.197
444
P RRT020 Rare Tumor 39 0.197
445
P TRM003 Tremor 50 0.197
446
FRG008 Fragile X-Associated Tremor/ataxia Syndrome 44 0.161
447
FML037 Female Breast Cancer 51 0.161
448
ARM001 Aromatase Deficiency 54 0.161
449
c THY107 Thymoma, Familial 42 0.161
450
c VTM027 Vitamin D-Dependent Rickets, Type 2a 54 0.161
451
FRG010 Fragile X Tremor/ataxia Syndrome 43 0.161
452
P SPP010 Suppressor of Tumorigenicity 3 50 0.161
453
ADR042 Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency 50 0.161
454
P ATX030 Ataxia-Telangiectasia 80 0.161
455
P AST005 Asthma 75 0.161
456
c FNC028 Fanconi Anemia, Complementation Group L 46 0.161
457
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 0.161
458
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 0.161
459
c CNG411 Congenital Disorder of Glycosylation, Type in 66 0.161
460
NND010 Nondisjunction 34 0.161
461
LNT004 Lentigines 45 0.161
462
c SPR118 Spermatogenic Failure 1 36 0.161
463
c HRD202 Hereditary Lymphedema I 54 0.161
464
THR024 Thrombosis 56 0.161
465
P SPN052 Spondyloarthropathy 54 0.161
466
OVR121 Ovarian Sex-Cord Stromal Tumor 32 0.161
467
P HYP069 Hyperparathyroidism 62 0.161
468
PST028 Post-Traumatic Stress Disorder 58 0.161
469
P THY023 Thymoma 64 0.161
470
URT037 Urethral Stricture 42 0.161
471
P LMY004 Leiomyosarcoma 62 0.161
472
THY020 Thyroid Hyalinizing Trabecular Adenoma 19 0.161
473
PLC009 Placenta Praevia 39 0.161
474
SNS003 Sensory Peripheral Neuropathy 51 0.161
475
EMB004 Embryonal Carcinoma 55 0.161
476
HYP066 Hyperglycemia 60 0.161
477
MLD002 Mild Pre-Eclampsia 33 0.161
478
c HPT003 Hepatitis a 63 0.161
479
BRD004 Borderline Personality Disorder 53 0.161
480
P DRM010 Dermatomyositis 61 0.161
481
TLN003 Telangiectasis 51 0.161
482
P MLN008 Melanoma 75 0.161
483
SPR018 Spermatocytoma 34 0.161
484
ACT084 Acute Stress Disorder 53 0.161
485
c INH020 Inherited Metabolic Disorder 47 0.161
486
TST010 Testicular Spermatocytic Seminoma 33 0.161
487
CNG486 Congenital Disorders of N-Linked Glycosylation and Multiple Pathway 29 0.161
488
PLM033 Pulmonary Embolism 58 0.161
489
PPT005 Peptic Ulcer Disease 58 0.161
490
CNG608 Congenital Hypopituitarism 29 0.161
491
HYD005 Hydrocele 46 0.161
492
46X012 46,xy Partial Gonadal Dysgenesis 41 0.161
493
FNC050 Functioning Gonadotropic Adenoma 26 0.161
494
RVR002 Reversible Cerebral Vasoconstriction Syndrome 32 0.161
495
DSR031 Disorder of Copper Metabolism 25 0.161
496
GLM044 Glomerular Disease 34 0.161
497
RRC029 Rare Cause of Hypertension 13 0.161
498
P HYP265 Hypotonia 42 0.161
499
P SCL018 Scoliosis 57 0.114
500
CRH005 Crohn's Colitis 53 0.114
501
ORL015 Oral Squamous Cell Carcinoma 43 0.114
502
FBR054 Fibroma 44 0.114
503
c ATM002 Autoimmune Polyendocrine Syndrome Type 1 43 0.114
504
DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 0.114
505
PLY150 Polykaryocytosis Inducer 29 0.114
506
c PSD108 Pseudohypoparathyroidism, Type Ia 64 0.114
507
c BRN108 Branchiootic Syndrome 1 63 0.114
508
AST006 Astigmatism 46 0.114
509
CRB081 Cerebellar Ataxia, Cayman Type 39 0.114
510
c 46X051 46,xy Sex Reversal 1 38 0.114
511
INT323 Intraocular Pressure Quantitative Trait Locus 63 0.114
512
P GST053 Gastric Cancer 82 0.114
513
HRL003 Hurler Syndrome 66 0.114
514
c NPH032 Nephronophthisis 4 46 0.114
515
P MCP040 Mucopolysaccharidosis-Plus Syndrome 70 0.114
516
KLP010 Klippel-Trenaunay-Weber Syndrome 59 0.114
517
c HYP836 Hypercholesterolemia, Familial, 1 73 0.114
518
HYP748 Hypertelorism 46 0.114
519
ESP021 Esophageal Cancer 84 0.114
520
ONC007 Oncocytoma 49 0.114
521
c BRS111 Breast-Ovarian Cancer, Familial 2 53 0.114
522
FBR009 Fibrous Dysplasia 48 0.114
523
CMB007 Combined Immunodeficiency 56 0.114
524
P LYD011 Leydig Cell Hypoplasia 35 0.114
525
P RCT021 Rectum Cancer 54 0.114
526
OST015 Osteochondrodysplasia 60 0.114
527
P TCD001 Tic Disorder 50 0.114
528
FML063 Familial Glucocorticoid Deficiency 58 0.114
529
CNS004 Constipation 56 0.114
530
LNG039 Lung Squamous Cell Carcinoma 57 0.114
531
HMT002 Hematologic Cancer 61 0.114
532
GRM004 Germinoma 40 0.114
533
c ACT068 Acute Cystitis 60 0.114
534
P HYP024 Hypoparathyroidism 55 0.114
535
P MCR010 Microcephaly 59 0.114
536
P ATM019 Autoimmune Polyendocrine Syndrome 46 0.114
537
BCT004 Bacteriuria 48 0.114
538
P ATS308 Autosomal Dominant Cerebellar Ataxia 64 0.114
539
PRT037 Pertussis 49 0.114
540
P END046 Endometritis 46 0.114
541
PLV003 Pelvic Inflammatory Disease 54 0.114
542
P RNL017 Renal Oncocytoma 54 0.114
543
GST029 Gastric Cardia Adenocarcinoma 30 0.114
544
c PRG011 Progressive Myoclonus Epilepsy 41 0.114
545
P DBT005 Diabetes Insipidus 54 0.114
546
c 46X060 46,xx Disorder of Sex Development 18 0.114
547
DFN038 Dfnb1 35 0.114
548
GGN002 Gigantism 32 0.114
549
OVR098 Ovarian Fibroma 24 0.114
550
c PST093 Posterior Hypospadias 19 0.114
551
P GNT133 Genetic Disorder of Sex Development 4 0.114
552
OVR097 Ovarian Fibrothecoma 29 0.114
553
CHR274 Chromosome Xq Duplication 12 0.114
554
DWR001 Dwarfism 44 0.114
555
P MYC026 Myoclonus Epilepsy 35 0.114
556
P MYC033 Myoclonus 46 0.114
557
PSD088 Pseudobulbar Affect 33 0.114
558
SPN186 Spinal Cord Injury 60 0.114
559
SXC004 Sex Chromosome Disorder of Sex Development 10 0.114
560
PRM329 Premature Aging 36 0.114
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