Search results for MYO9A

21 hits were found for MYO9A

# Family MCID Name MIFTS Score
1
c MYS081 Myasthenic Syndrome, Congenital, 24, Presynaptic 21 5.170
2
P CNG001 Congenital Myasthenic Syndrome 66 4.868
3
P BRD002 Bardet-Biedl Syndrome 66 3.762
4
P CHR654 Charcot-Marie-Tooth Disease, Axonal, Type 2e 59 3.033
5
P PRS124 Presynaptic Congenital Myasthenic Syndromes 36 2.321
6
c BRD019 Bardet-Biedl Syndrome 7 43 2.145
7
c SPN214 Spinocerebellar Ataxia, Autosomal Recessive 10 42 2.145
8
c MYS078 Myasthenic Syndrome, Congenital, 14 39 2.145
9
CHR381 Chromosome 17q23.1-Q23.2 Deletion Syndrome 34 2.145
10
c MYP098 Myopathy, Centronuclear, 4 33 2.145
11
c MYP118 Myopathy, Myofibrillar, 8 31 2.145
12
c MYP119 Myopathy, Myofibrillar, 7 30 2.145
13
c MYP148 Myopathy, Centronuclear, 5 30 2.145
14
P RTN008 Retinitis Pigmentosa 79 0.088
15
CHR619 Chromosome 2q35 Duplication Syndrome 62 0.088
16
P PLY006 Polydactyly 59 0.088
17
P RTN016 Retinal Degeneration 53 0.088
18
ATS010 Autosomal Recessive Disease 48 0.088
19
RTN023 Retinitis 46 0.088
20
c BRD016 Bardet-Biedl Syndrome 4 46 0.088
21
NRR001 Neuroretinitis 42 0.088
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