Search results for oca2

23 hits were found for oca2

# Family MCID Name MIFTS Score
1
c ALB021 Albinism, Oculocutaneous, Type Ii 49 18.950
2
ALB002 Albinism 45 6.531
3
P OCL002 Oculocutaneous Albinism 55 6.431
4
P CNG024 Congenital Nystagmus 39 3.663
5
OCL001 Ocular Albinism 43 3.616
6
P GLY010 Glycine Encephalopathy 53 2.952
7
c HRM005 Hermansky-Pudlak Syndrome 1 52 2.952
8
DYS022 Dyschromatosis Symmetrica Hereditaria 46 2.952
9
ACT011 Acute Contagious Conjunctivitis 35 2.952
10
PNN005 Panencephalitis, Subacute Sclerosing 32 2.952
11
c ACT067 Acute Conjunctivitis 31 2.952
12
BRW007 Brown Oca 9 2.952
13
c PRD028 Prader-Willi Syndrome Due to Maternal Uniparental Disomy of Chromosome 15 14 2.160
14
c PRD022 Prader-Willi Syndrome Due to Paternal Deletion of 15q11q13 Type 1 12 2.160
15
c PRD023 Prader-Willi Syndrome Due to Paternal Deletion of 15q11q13 Type 2 12 2.160
16
c ANG053 Angelman Syndrome Due to Maternal 15q11q13 Deletion 9 2.160
17
MLN008 Melanoma 70 0.175
18
c ALB009 Albinism, Oculocutaneous, Type Ia 37 0.152
19
P BRS047 Breast Cancer 100 0.088
20
P ANG001 Angelman Syndrome 62 0.088
21
SCK005 Sickle Cell Disease 51 0.088
22
c EST002 Estrogen-Receptor Negative Breast Cancer 41 0.088
23
c ALB020 Albinism, Oculocutaneous, Type Iii 28 0.088
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