Search results for pou3f4

91 hits were found for pou3f4

# Family MCID Name MIFTS Score
1
DFN013 Deafness Mixed with Perilymphatic Gusher, X-Linked 22 47.470
2
c DFN036 Deafness, X-Linked 2 44 46.180
3
RRG078 Rare Genetic Deafness 38 24.822
4
P SNS001 Sensorineural Hearing Loss 60 16.611
5
HRD199 Hereditary Hearing Loss and Deafness 25 15.164
6
P NNS072 Nonsyndromic Hearing Loss 42 12.281
7
c XLN004 X-Linked Nonsyndromic Deafness 28 11.965
8
DFN245 Deafness, Autosomal Recessive 4, with Enlarged Vestibular Aqueduct 52 9.905
9
CHR506 Choroideremia, Deafness, and Mental Retardation 27 9.366
10
CHR081 Choroideremia 58 8.294
11
P DFN349 Deafness, Nonsyndromic Sensorineural, Mitochondrial 35 8.160
12
c DFN186 Deafness, Y-Linked 1 26 8.092
13
NRR002 Norrie Disease 59 7.287
14
c DFN194 Deafness, X-Linked 1 35 7.287
15
c DFN147 Deafness, X-Linked 4 33 7.287
16
MHR001 Mohr-Tranebjaerg Syndrome 49 7.235
17
P USH001 Usher Syndrome 63 7.235
18
PND002 Pendred Syndrome 57 7.235
19
DFN380 Deafness, X-Linked 5, with Peripheral Neuropathy 36 7.167
20
MNT146 Mental Retardation, X-Linked, Syndromic, Martin-Probst Type 32 7.167
21
c DFN276 Deafness, X-Linked 6 29 7.167
22
c DFN146 Deafness, X-Linked 3 27 7.167
23
c DFN092 Deafness, Autosomal Recessive 49 38 7.167
24
P WRD001 Waardenburg's Syndrome 60 7.167
25
P YLN002 Y-Linked Monogenic Disease 17 7.004
26
c ATS005 Autosomal Dominant Nonsyndromic Deafness 24 7.004
27
PRT052 Partington X-Linked Mental Retardation Syndrome 44 7.004
28
c CHR408 Charcot-Marie-Tooth Disease, X-Linked Recessive, 5 43 7.004
29
c DFN117 Deafness, Autosomal Dominant 15 37 7.004
30
ART002 Arts Syndrome 66 7.004
31
XLN230 X-Linked Monogenic Disease 20 7.004
32
c DFN103 Deafness, Autosomal Recessive 1b 40 7.004
33
ADT003 Auditory System Disease 48 7.004
34
SPL007 Splenic Abscess 30 7.004
35
CHR079 Choroid Disease 37 7.004
36
P YLN003 Y-Linked Deafness 20 7.004
37
c BRN108 Branchiootic Syndrome 1 63 6.781
38
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 4.854
39
c NNS007 Nonsyndromic Deafness 36 1.750
40
CLL010 Cellular Ependymoma 58 1.577
41
TNY001 Tanycytic Ependymoma 29 1.577
42
PPL013 Papillary Ependymoma 30 1.577
43
CLR011 Clear Cell Ependymoma 31 1.577
44
ERM002 Ear Malformation 37 1.205
45
HLX001 Helix Syndrome 47 1.205
46
HYP748 Hypertelorism 46 1.170
47
CRB079 Cerebrospinal Fluid Leak 35 1.088
48
DFN313 Deafness-Hypogonadism Syndrome 24 0.890
49
P PNC035 Pancreatic Cancer 87 0.642
50
c WLF013 Wolfram Syndrome 1 60 0.327
51
c USH036 Usher Syndrome, Type I 60 0.283
52
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 0.283
53
ATS252 Autosomal Recessive Non-Syndromic Sensorineural Deafness Type Dfnb 42 0.283
54
CNG410 Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly 60 0.231
55
c MLT156 Multiple Endocrine Neoplasia, Type I 71 0.231
56
P MLT074 Multiple Endocrine Neoplasia 58 0.231
57
INS001 Insulinoma 59 0.231
58
HYP231 Hypothalamic Hamartomas 33 0.231
59
VLC001 Velocardiofacial Syndrome 57 0.163
60
c WRD030 Waardenburg Syndrome, Type 1 54 0.163
61
P MDL005 Medulloblastoma 75 0.163
62
c SML038 Small Cell Cancer of the Lung 68 0.163
63
DGR001 Digeorge Syndrome 62 0.163
64
c OTP006 Otopalatodigital Syndrome, Type I 59 0.163
65
P ANR048 Aniridia 1 66 0.163
66
CFF002 Coffin-Lowry Syndrome 59 0.163
67
P CFF008 Coffin-Siris Syndrome 1 63 0.163
68
c USH041 Usher Syndrome, Type if 47 0.163
69
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 0.163
70
P BRT053 Bartter Syndrome, Type 4a, Neonatal, with Sensorineural Deafness 45 0.163
71
c DFN203 Deafness, Autosomal Recessive 30 41 0.163
72
CRN264 Craniosynostosis with Fibular Aplasia 29 0.163
73
KRT019 Keratitis, Hereditary 66 0.163
74
P FRG001 Fragile X Syndrome 70 0.163
75
RTN187 Retinitis Pigmentosa-Deafness Syndrome 48 0.163
76
c USH040 Usher Syndrome, Type Id 47 0.163
77
CLF027 Cleft Palate, Isolated 64 0.163
78
c DFN178 Deafness, Autosomal Recessive 59 32 0.163
79
CHR593 Chromosome 16p13.3 Deletion Syndrome, Proximal 68 0.163
80
c DFN201 Deafness, Autosomal Recessive 3 37 0.163
81
PNC001 Pancytopenia 52 0.163
82
KRT009 Keratosis 52 0.163
83
P ICH004 Ichthyosis 56 0.163
84
P DYS154 Dystonia 64 0.163
85
AMN001 Amenorrhea 53 0.163
86
PLY012 Polyhydramnios 46 0.163
87
c BRT024 Bartter Syndrome Type 4 25 0.163
88
MND005 Mondini Dysplasia 18 0.163
89
GRW007 Growth Hormone Deficiency 47 0.163
90
NNS044 Non-Syndromic Genetic Deafness 38 0.163
91
P RRD005 Rare Deafness 20 0.163
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