Search results for SRY

183 hits were found for SRY

# Family MCID Name MIFTS Score
1
c 46X051 46,xy Sex Reversal 1 44 21.250
2
P 46X052 46,xx Sex Reversal 1 50 18.675
3
c 46X082 46,xy Sex Reversal 46 4.277
4
P GND004 Gonadal Dysgenesis 48 4.199
5
c 46X059 46,xx Sex Reversal 4 22 4.088
6
P TRN020 Turner Syndrome 67 3.573
7
c 46X081 46,xx Sex Reversal 34 3.418
8
GND001 Gonadoblastoma 44 2.989
9
HRM002 Hermaphroditism 36 2.978
10
P HYP040 Hypospadias 51 2.956
11
P CMP005 Campomelic Dysplasia 64 2.869
12
P MXD016 Mixed Gonadal Dysgenesis 35 2.824
13
P MLN007 Male Infertility 55 2.791
14
AND002 Androgen Insensitivity Syndrome 66 2.772
15
GYN001 Gynecomastia 49 2.772
16
NNS035 Nonsyndromic 46,xx Testicular Disorders of Sex Development 11 2.175
17
47X002 47,xyy 49 2.106
18
DYS101 Dysgerminoma 44 2.038
19
FRS002 Frasier Syndrome 55 1.997
20
c 46X079 46,xy Sex Reversal 11 39 1.973
21
c WLM013 Wilms Tumor 1 65 1.946
22
PSD009 Pseudohermaphroditism 46 1.946
23
46X012 46,xy Partial Gonadal Dysgenesis 37 1.946
24
ANR018 Anorchia 36 1.946
25
NNS042 Nonsyndromic Disorders of Testicular Development 21 1.946
26
CMP034 Complete Androgen Insensitivity Syndrome 46 1.915
27
LRW001 Leri-Weill Dyschondrosteosis 43 1.915
28
c 45X001 45,x/46,xy Mixed Gonadal Dysgenesis 33 1.915
29
P DSR089 Disorders of Sexual Development 45 0.322
30
P INF032 Infertility 57 0.266
31
c 46X011 46, Xy Disorders of Sexual Development 20 0.225
32
AZS001 Azoospermia 50 0.213
33
HYP080 Hypogonadism 50 0.188
34
CRY035 Cryptorchidism, Unilateral or Bilateral 58 0.174
35
AMN001 Amenorrhea 54 0.174
36
c WLM018 Wilms Tumor 5 61 0.159
37
HLX001 Helix Syndrome 47 0.123
38
INF021 Infant Gynecomastia 31 0.112
39
P NRB001 Neuroblastoma 72 0.101
40
P SYN140 Syndrome with 46,xy Disorder of Sex Development 23 0.101
41
P GST053 Gastric Cancer 83 0.087
42
LPD012 Lipoid Congenital Adrenal Hyperplasia 70 0.087
43
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.087
44
DNY001 Denys-Drash Syndrome 57 0.087
45
EMB004 Embryonal Carcinoma 56 0.087
46
c 46X049 46,xy Sex Reversal 2 48 0.087
47
SMN007 Seminoma 43 0.087
48
PLM173 Palmoplantar Hyperkeratosis with Squamous Cell Carcinoma of Skin and 46,xx Sex Reversal 34 0.087
49
c 46X060 46,xx Disorder of Sex Development 18 0.087
50
P HPT023 Hepatocellular Carcinoma 100 0.071
51
P CLR023 Colorectal Cancer 99 0.071
52
NRL016 Neural Tube Defects 82 0.071
53
P ATS364 Autism 70 0.071
54
P HRS035 Hirschsprung Disease 1 65 0.071
55
P ADN016 Adenocarcinoma 64 0.071
56
c PRC016 Pre-Eclampsia 63 0.071
57
CHR619 Chromosome 2q35 Duplication Syndrome 62 0.071
58
ALC006 Alcoholic Hepatitis 61 0.071
59
THY029 Thyroid Carcinoma 59 0.071
60
P INS002 in Situ Carcinoma 53 0.071
61
P HYP730 Hypogonadotropic Hypogonadism 52 0.071
62
CHR074 Choriocarcinoma 47 0.071
63
LYD001 Leydig Cell Tumor 45 0.071
64
c 46X055 46,xy Sex Reversal 3 40 0.071
65
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.071
66
GST052 Gestational Choriocarcinoma 36 0.071
67
TST043 Testicular Seminoma 35 0.071
68
CHR178 Chromosomal Triplication 35 0.071
69
HRZ001 Huriez Syndrome 31 0.071
70
c 46X048 46,xx Sex Reversal 2 27 0.071
71
BCR002 Bicornuate Uterus 24 0.071
72
UBQ002 Ubiquitin-Activating Enzyme, Y-Linked 8 0.071
73
P LNG032 Lung Cancer 98 0.050
74
P PRS040 Prostate Cancer 97 0.050
75
P BRS047 Breast Cancer 97 0.050
76
ESP021 Esophageal Cancer 90 0.050
77
c LKM061 Leukemia, Acute Myeloid 84 0.050
78
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.050
79
P RTT002 Rett Syndrome 80 0.050
80
P BLD134 Bladder Cancer 79 0.050
81
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.050
82
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.050
83
c ART115 Aortic Valve Disease 1 75 0.050
84
END057 Endometrial Cancer 74 0.050
85
P OST002 Osteoporosis 74 0.050
86
P RTN024 Retinoblastoma 73 0.050
87
P KDN018 Kidney Disease 72 0.050
88
GST040 Gastric Adenocarcinoma 70 0.050
89
MYL009 Myelodysplastic Syndrome 70 0.050
90
P MLN008 Melanoma 69 0.050
91
P LVR013 Liver Disease 68 0.050
92
P SYS005 Systemic Scleroderma 68 0.050
93
c ATS007 Autism Spectrum Disorder 67 0.050
94
c PRM196 Premature Ovarian Failure 1 67 0.050
95
ACH004 Achondroplasia 66 0.050
96
CRN036 Craniopharyngioma 65 0.050
97
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.050
98
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.050
99
ATH013 Atherosclerosis Susceptibility 65 0.050
100
CLR108 Colorectal Adenoma 64 0.050
101
DGR001 Digeorge Syndrome 64 0.050
102
P GLM045 Glioma 63 0.050
103
c ALP101 Alpha-Thalassemia 62 0.050
104
c SVR001 Severe Acute Respiratory Syndrome 62 0.050
105
ALL026 Allergic Hypersensitivity Disease 62 0.050
106
HSH003 Hashimoto Thyroiditis 62 0.050
107
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.050
108
FTT001 Fatty Liver Disease 61 0.050
109
P SCL018 Scoliosis 60 0.050
110
ING001 Inguinal Hernia 60 0.050
111
P THL005 Thalassemia 60 0.050
112
SPP011 Suppression of Tumorigenicity 12 59 0.050
113
WLF002 Wolf-Hirschhorn Syndrome 59 0.050
114
P WRD001 Waardenburg's Syndrome 59 0.050
115
ADN018 Adenoma 59 0.050
116
MCR013 Microphthalmia 57 0.050
117
PLC005 Placental Insufficiency 57 0.050
118
P NRF002 Neurofibromatosis 56 0.050
119
AND020 Androgen Insensitivity, Partial 56 0.050
120
c THY109 Thyroid Cancer, Nonmedullary, 1 56 0.050
121
PTS001 Patau Syndrome 55 0.050
122
PRS045 Prostatic Hypertrophy 53 0.050
123
P RNL017 Renal Oncocytoma 53 0.050
124
c FML008 Familial Retinoblastoma 53 0.050
125
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.050
126
P SML001 Small Cell Carcinoma 52 0.050
127
IMP005 Impotence 52 0.050
128
c TRC092 Trichorhinophalangeal Syndrome, Type I 52 0.050
129
P THY032 Thyroiditis 52 0.050
130
TLN003 Telangiectasis 52 0.050
131
P THR015 Thrombophilia 51 0.050
132
PRP066 Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, and Hirschsprung Disease 51 0.050
133
END086 End Stage Renal Disease 51 0.050
134
c HRD202 Hereditary Lymphedema I 50 0.050
135
PLC008 Placenta Disease 50 0.050
136
PRS129 Prostatic Hyperplasia, Benign 49 0.050
137
c HPT015 Hepatitis D 49 0.050
138
HYP043 Hyperandrogenism 48 0.050
139
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.050
140
CYS002 Cystic Lymphangioma 48 0.050
141
SXL003 Sexual Disorder 47 0.050
142
THY128 Thyroid Tumor 47 0.050
143
PLM029 Palmoplantar Keratosis 47 0.050
144
P CRC039 Coarctation of Aorta 47 0.050
145
HYD005 Hydrocele 46 0.050
146
MGC001 Megacolon 46 0.050
147
c MLG068 Malignant Glioma 46 0.050
148
SVN002 Sveinsson Chorioretinal Atrophy 46 0.050
149
GLL048 Glial Tumor 45 0.050
150
SGN002 Signet Ring Cell Adenocarcinoma 45 0.050
151
TRT001 Teratocarcinoma 45 0.050
152
c WRD024 Waardenburg Syndrome, Type 4c 45 0.050
153
DWR001 Dwarfism 44 0.050
154
P HYP265 Hypotonia 43 0.050
155
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.050
156
P HYP087 Hypotrichosis 42 0.050
157
KLD004 Keloid Disorder 40 0.050
158
P SPR119 Spermatogenic Failure, X-Linked, 1 39 0.050
159
SRT003 Sertoli-Leydig Cell Tumor 38 0.050
160
HPT070 Hepatosplenic T-Cell Lymphoma 38 0.050
161
P CRB059 Cerebellar Degeneration 37 0.050
162
PRT049 Partial Deletion of Y 33 0.050
163
LTM002 Luteoma 32 0.050
164
48X003 48,xxyy Syndrome 31 0.050
165
LMB069 Lamb-Shaffer Syndrome 31 0.050
166
EMB006 Embryonal Testis Carcinoma 31 0.050
167
CHR075 Choriocarcinoma of Ovary 31 0.050
168
c WRD010 Waardenburg Syndrome Type 4 29 0.050
169
ARG004 Argyria 27 0.050
170
NNG002 Non-Gestational Ovarian Choriocarcinoma 25 0.050
171
c DMN005 Diamond-Blackfan Anemia 2 25 0.050
172
48X002 48,xxxy Syndrome 24 0.050
173
GST035 Gestational Ovarian Choriocarcinoma 23 0.050
174
FRM001 Freemartinism 22 0.050
175
CHR247 Chromosome 4p Deletion 22 0.050
176
MCR330 Microphthalmia, Isolated, with Cataract 1 19 0.050
177
CTN020 Cutaneous Sclerosis 17 0.050
178
ISL133 Isolated Epispadias 16 0.050
179
DPL003 Diploid-Triploid Mosaicism 14 0.050
180
RCT033 Rectal Duplication 13 0.050
181
SHX003 Shox Deficiency Disorders 12 0.050
182
TST045 Testes, Rudimentary 9 0.050
183
P ISC012 Isochromosome Y 7 0.050
Content
Loading form....