Search results for oca2

28 hits were found for oca2

# Family MCID Name MIFTS Score
1
c ALB021 Albinism, Oculocutaneous, Type Ii 47 18.848
2
ALB002 Albinism 45 6.416
3
P OCL002 Oculocutaneous Albinism 57 5.963
4
c SKN065 Skin/hair/eye Pigmentation, Variation in, 1 23 3.739
5
P CNG024 Congenital Nystagmus 40 3.601
6
P OCL001 Ocular Albinism 46 3.556
7
P PRD006 Prader-Willi Syndrome 66 2.904
8
P GLY010 Glycine Encephalopathy 52 2.904
9
DYS022 Dyschromatosis Symmetrica Hereditaria 49 2.904
10
c HRM005 Hermansky-Pudlak Syndrome 1 47 2.904
11
PNN005 Panencephalitis, Subacute Sclerosing 44 2.904
12
ACT011 Acute Contagious Conjunctivitis 40 2.904
13
c ACT067 Acute Conjunctivitis 32 2.904
14
c PRD028 Prader-Willi Syndrome Due to Maternal Uniparental Disomy of Chromosome 15 17 2.122
15
c PRD022 Prader-Willi Syndrome Due to Paternal Deletion of 15q11q13 Type 1 13 2.122
16
c PRD023 Prader-Willi Syndrome Due to Paternal Deletion of 15q11q13 Type 2 13 2.122
17
c ANG053 Angelman Syndrome Due to Maternal 15q11q13 Deletion 9 2.122
18
c BLD140 Blood Group, I System 37 0.301
19
MLN008 Melanoma 72 0.167
20
c ALB009 Albinism, Oculocutaneous, Type Ia 41 0.144
21
P MLN066 Melanoma, Cutaneous Malignant 1 60 0.118
22
DLT018 Dilution, Pigmentary 37 0.118
23
P BRS047 Breast Cancer 100 0.083
24
P ANG001 Angelman Syndrome 61 0.083
25
SCK005 Sickle Cell Disease 54 0.083
26
c EST002 Estrogen-Receptor Negative Breast Cancer 44 0.083
27
c ALB019 Albinism, Oculocutaneous, Type Iv 30 0.083
28
c ALB020 Albinism, Oculocutaneous, Type Iii 29 0.083
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