Search results for DIAPH1

36 hits were found for DIAPH1

# Family MCID Name MIFTS Score
1
c DFN131 Deafness, Autosomal Dominant 1 45 8.619
2
SZR027 Seizures, Cortical Blindness, and Microcephaly Syndrome 29 7.182
3
P MCR010 Microcephaly 59 4.658
4
P SNS001 Sensorineural Hearing Loss 60 3.638
5
CRT012 Cortical Blindness 37 3.497
6
P SZR006 Seizure Disorder 56 3.015
7
RRG078 Rare Genetic Deafness 29 2.982
8
P NNS072 Nonsyndromic Hearing Loss 41 2.904
9
P THR014 Thrombocytopenia 67 2.855
10
c USH036 Usher Syndrome, Type I 60 2.855
11
c DFN351 Deafness, Autosomal Dominant 6 42 2.083
13
c ADT007 Auditory Neuropathy, Autosomal Dominant, 1 35 2.019
14
c DFN284 Deafness, Autosomal Dominant 67 31 2.019
15
c ATS005 Autosomal Dominant Nonsyndromic Deafness 26 2.019
16
c DFN272 Deafness, Autosomal Dominant 54 24 2.019
17
HRD199 Hereditary Hearing Loss and Deafness 21 2.019
18
c BRN108 Branchiootic Syndrome 1 62 0.155
19
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.155
20
P CLR023 Colorectal Cancer 99 0.109
21
ATS251 Autosomal Dominant Non-Syndromic Sensorineural Deafness Type Dfna 31 0.109
22
STR067 Stroke, Ischemic 81 0.077
23
SVR004 Severe Combined Immunodeficiency 73 0.077
24
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.077
25
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.077
26
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.077
27
P GLM045 Glioma 63 0.077
28
SQM006 Squamous Cell Carcinoma 60 0.077
29
P BRN022 Bronchiectasis 59 0.077
30
VSL002 Visual Epilepsy 59 0.077
31
ISC004 Ischemia 58 0.077
32
P NRP001 Neuropathy 56 0.077
33
GLL048 Glial Tumor 45 0.077
34
SYN005 Synostosis 45 0.077
35
LRY018 Laryngeal Squamous Cell Carcinoma 44 0.077
36
P ADT009 Auditory Neuropathy Spectrum Disorder 36 0.077
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