Search results for AMH

172 hits were found for AMH

# Family MCID Name MIFTS Score
1
c PRS128 Persistent Mullerian Duct Syndrome, Types I and Ii 42 4.157
2
P PRS049 Persistent Mullerian Duct Syndrome 50 3.597
3
P PLY011 Polycystic Ovary Syndrome 56 3.257
4
P HYP730 Hypogonadotropic Hypogonadism 52 2.729
5
OVR029 Ovarian Hyperstimulation Syndrome 64 2.424
6
CRY035 Cryptorchidism, Unilateral or Bilateral 58 2.321
7
P OVR049 Ovarian Disease 52 2.199
8
P GND004 Gonadal Dysgenesis 48 2.199
9
P TRN020 Turner Syndrome 67 2.158
10
VRC001 Varicocele 49 2.158
11
MCC012 Mccune-Albright Syndrome 70 2.134
12
MYM001 Myoma 54 2.108
13
P TRT010 Teratoma 52 2.108
14
PSD009 Pseudohermaphroditism 46 2.108
15
P GLC113 Galactosemia I 64 2.076
16
c BNG093 Benign Teratoma 37 2.076
17
P MXD016 Mixed Gonadal Dysgenesis 35 2.076
18
ANV001 Anovulation 47 1.728
19
c PRM196 Premature Ovarian Failure 1 67 1.632
20
ING001 Inguinal Hernia 60 1.613
21
P OVR046 Ovarian Cyst 47 1.613
22
P DSR089 Disorders of Sexual Development 45 1.613
23
LPD012 Lipoid Congenital Adrenal Hyperplasia 70 1.541
24
P KLL001 Kallmann Syndrome 61 1.509
25
END011 Endometriosis of Ovary 39 1.509
26
HRM002 Hermaphroditism 36 1.509
27
FRM001 Freemartinism 22 1.509
28
AND002 Androgen Insensitivity Syndrome 66 1.468
29
c 46X049 46,xy Sex Reversal 2 48 1.468
30
TST044 Testicular Torsion 47 1.468
31
c 46X082 46,xy Sex Reversal 46 1.468
32
MLL011 Mullerian Aplasia and Hyperandrogenism 46 1.468
33
OLG001 Oligospermia 45 1.468
34
GND001 Gonadoblastoma 44 1.468
35
SXC001 Sex Cord-Gonadal Stromal Tumor 43 1.468
36
TST015 Testicular Disease 43 1.468
37
c 46X030 46,xy Sex Reversal 9 42 1.468
38
PRM013 Premature Menopause 41 1.468
39
c 46X002 46 Xx Gonadal Dysgenesis 41 1.468
40
SBC017 Sebaceous Gland Disease 40 1.468
41
PST029 Postmenopausal Atrophic Vaginitis 38 1.468
42
P SLP003 Salpingitis 38 1.468
43
ADH001 Adhesions of Uterus 36 1.468
44
OLG022 Oligoasthenoteratozoospermia 36 1.468
45
PLV004 Pelvic Varices 34 1.468
46
c 46X081 46,xx Sex Reversal 34 1.468
47
P INH011 Inherited Bone Marrow Failure Syndromes 34 1.468
48
c 45X001 45,x/46,xy Mixed Gonadal Dysgenesis 33 1.468
49
MXL016 Maxillonasal Dysplasia, Binder Type 32 1.468
50
STR018 Steroid Inherited Metabolic Disorder 31 1.468
51
OVR041 Ovarian Benign Neoplasm 30 1.468
52
DRM005 Dermoid Cyst of Ovary 30 1.468
53
UTR031 Uterine Benign Neoplasm 29 1.468
54
RPR001 Reproductive Organ Benign Neoplasm 28 1.468
55
OVR005 Ovarian Large-Cell Neuroendocrine Carcinoma 27 1.468
56
OVR057 Ovarian Serous Adenofibroma 27 1.468
57
OVR002 Ovarian Serous Cystadenofibroma 27 1.468
58
INT013 Intramuscular Hemangioma 26 1.468
59
SLP002 Salpingitis Isthmica Nodosa 24 1.468
60
c CHR018 Chronic Salpingo-Oophoritis 23 1.468
61
P SLP004 Salpingo-Oophoritis 22 1.468
62
SBS001 Subserous Uterine Fibroid 20 1.468
63
TST005 Testicular Gonadoblastoma 19 1.468
64
P INF032 Infertility 57 0.254
65
HYP080 Hypogonadism 50 0.200
66
HYP043 Hyperandrogenism 48 0.200
67
P END044 Endometriosis 63 0.158
68
AMN001 Amenorrhea 54 0.141
69
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.132
70
c PLY105 Polycystic Ovary Syndrome 1 38 0.122
71
ANR018 Anorchia 36 0.122
72
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.112
73
P HYP086 Hypothyroidism 69 0.100
74
AZS001 Azoospermia 50 0.100
75
c NRF023 Neurofibromatosis, Type Ii 80 0.086
76
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.086
77
P VSC007 Vascular Disease 63 0.086
78
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.086
79
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.086
80
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.086
81
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.086
82
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.086
83
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.086
84
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.086
85
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.086
86
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.086
87
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.086
88
c CNG562 Congenital Hypogonadotropic Hypogonadism 34 0.086
89
ART016 Aortic Aneurysm 69 0.071
90
c RHB024 Rhabdomyosarcoma 2 67 0.071
91
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.071
92
HYP020 Hyperprolactinemia 64 0.071
93
c PRC016 Pre-Eclampsia 63 0.071
94
c WLM018 Wilms Tumor 5 61 0.071
95
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.071
96
P HYP535 Hypogonadotropic Hypogonadism 7 with or Without Anosmia 59 0.071
97
MYR002 Mayer-Rokitansky-Kuster-Hauser Syndrome 58 0.071
98
MBS002 Moebius Syndrome 57 0.071
99
P ALP008 Alopecia 54 0.071
100
P ALP061 Alopecia, Androgenetic, 1 49 0.071
101
P PRC019 Precocious Puberty 46 0.071
102
c CNT075 Central Precocious Puberty 46 0.071
103
AND014 Androgenic Alopecia 46 0.071
104
P OCY003 Oocyte Maturation Defect 1 45 0.071
105
P VND001 Vein Disease 42 0.071
106
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.071
107
ISL004 Isolated Gonadotropin-Releasing Hormone Deficiency 26 0.071
108
P BRS047 Breast Cancer 97 0.050
109
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.050
110
CYS001 Cystic Fibrosis 81 0.050
111
CNN003 Conn's Syndrome 79 0.050
112
SCK003 Sickle Cell Anemia 74 0.050
113
LPT014 Leptin Deficiency or Dysfunction 74 0.050
114
ANX010 Anxiety 73 0.050
115
DWN001 Down Syndrome 70 0.050
116
P FRG001 Fragile X Syndrome 70 0.050
117
RCK004 Rickets 68 0.050
118
HYP056 Hypoglycemia 66 0.050
119
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.050
120
c WLM013 Wilms Tumor 1 65 0.050
121
P CMP005 Campomelic Dysplasia 64 0.050
122
ART002 Arts Syndrome 64 0.050
123
c ACT068 Acute Cystitis 63 0.050
124
LPD008 Lipid Metabolism Disorder 62 0.050
125
HSH003 Hashimoto Thyroiditis 62 0.050
126
MDD011 Mood Disorder 62 0.050
127
P INT143 Interstitial Cystitis 61 0.050
128
DPH001 Diphtheria 60 0.050
129
P TXP001 Toxoplasmosis 60 0.050
130
P ALP009 Alopecia Areata 60 0.050
131
ETN001 Eating Disorder 60 0.050
132
THY029 Thyroid Carcinoma 59 0.050
133
P SLP005 Sleep Disorder 59 0.050
134
SPS150 Spastic Ataxia, Charlevoix-Saguenay Type 58 0.050
135
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.050
136
BLR008 Bilirubin Metabolic Disorder 57 0.050
137
HMT008 Hematuria, Benign Familial 56 0.050
138
LMY014 Leiomyoma, Uterine 56 0.050
139
ADN027 Adenomyosis 56 0.050
140
AND020 Androgen Insensitivity, Partial 56 0.050
141
AGN016 Aging 56 0.050
142
P ACT010 Acth-Secreting Pituitary Adenoma 55 0.050
143
HYP060 Hyperinsulinism 54 0.050
144
GLC003 Glucose Intolerance 54 0.050
145
ADR049 Adrenal Hypoplasia, Congenital 54 0.050
146
ACR041 Acromelic Frontonasal Dysostosis 52 0.050
147
P THY032 Thyroiditis 52 0.050
148
LMY002 Leiomyoma 52 0.050
149
P HYP040 Hypospadias 51 0.050
150
ADR042 Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency 50 0.050
151
ECT026 Ectopic Pregnancy 50 0.050
152
47X002 47,xyy 49 0.050
153
ATS010 Autosomal Recessive Disease 48 0.050
154
TST014 Testicular Cancer 46 0.050
155
MYF001 Myofibroma 45 0.050
156
HYP784 Hypogonadism, Male 40 0.050
157
c 46X055 46,xy Sex Reversal 3 40 0.050
158
PLY100 Polyploidy 40 0.050
159
P SPR119 Spermatogenic Failure, X-Linked, 1 39 0.050
160
c 46X079 46,xy Sex Reversal 11 39 0.050
161
CHR178 Chromosomal Triplication 35 0.050
162
PPL052 Papillomatosis, Confluent and Reticulated 33 0.050
163
c 46X048 46,xx Sex Reversal 2 27 0.050
164
c PRM094 Premature Ovarian Failure 5 24 0.050
165
c 46X058 46,xy Sex Reversal 10 24 0.050
166
LYM053 Lymphomatous Thyroiditis 22 0.050
167
GND014 Gonadal Dysgenesis, Dysmorphic Facies, Retinal Dystrophy, and Myopathy 21 0.050
168
TST035 Testicular Anomalies with or Without Congenital Heart Disease 20 0.050
169
c PRM295 Premature Ovarian Failure 15 20 0.050
170
GLC025 Galactorrhoea-Hyperprolactinaemia 20 0.050
171
c OVR120 Ovarian Dysgenesis 8 20 0.050
172
RTN191 Retinal Dystrophy with or Without Extraocular Anomalies 19 0.050
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