Search results for AP1B1

15 hits were found for AP1B1

# Family MCID Name MIFTS Score
1
c KRT078 Keratitis-Ichthyosis-Deafness Syndrome, Autosomal Recessive 27 6.571
2
P ICH004 Ichthyosis 54 5.124
3
MNT317 Mental Retardation, Enteropathy, Deafness, Peripheral Neuropathy, Ichthyosis, and Keratoderma 43 3.673
4
c MNN043 Meningioma, Familial 74 2.520
5
MNN042 Meningioma, Radiation-Induced 62 2.520
6
c BRN108 Branchiootic Syndrome 1 62 0.132
7
SNS003 Sensory Peripheral Neuropathy 54 0.132
8
P KRT028 Keratitis-Ichthyosis-Deafness Syndrome, Autosomal Dominant 53 0.132
9
WLS001 Wilson Disease 71 0.093
10
P THR014 Thrombocytopenia 67 0.093
11
MNK001 Menkes Disease 64 0.093
12
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.093
13
P PRP019 Peripheral Nervous System Disease 58 0.093
14
P NRP001 Neuropathy 56 0.093
15
ATS010 Autosomal Recessive Disease 48 0.093
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