Search results for oca2

24 hits were found for oca2

# Family MCID Name MIFTS Score
1
c ALB021 Albinism, Oculocutaneous, Type Ii 47 19.577
2
ALB002 Albinism 46 6.253
3
P OCL002 Oculocutaneous Albinism 54 6.152
4
P CNG024 Congenital Nystagmus 40 4.032
5
OCL001 Ocular Albinism 42 3.991
6
c PRD028 Prader-Willi Syndrome Due to Maternal Uniparental Disomy of Chromosome 15 14 3.503
7
c PRD022 Prader-Willi Syndrome Due to Paternal Deletion of 15q11q13 Type 1 12 3.503
8
c PRD023 Prader-Willi Syndrome Due to Paternal Deletion of 15q11q13 Type 2 12 3.503
9
c ANG053 Angelman Syndrome Due to Maternal 15q11q13 Deletion 10 3.503
10
P GLY010 Glycine Encephalopathy 53 3.456
11
c HRM005 Hermansky-Pudlak Syndrome 1 49 3.456
12
DYS022 Dyschromatosis Symmetrica Hereditaria 46 3.456
13
ACT011 Acute Contagious Conjunctivitis 37 3.456
14
PNN005 Panencephalitis, Subacute Sclerosing 33 3.456
15
c ACT067 Acute Conjunctivitis 32 3.456
16
c ALB009 Albinism, Oculocutaneous, Type Ia 42 3.002
17
P ANG001 Angelman Syndrome 61 2.877
18
MLG108 Malignant Melanoma, Somatic 60 2.822
19
BRW007 Brown Oca 7 2.822
20
c PNC108 Pancreatitis, Hereditary 58 1.995
21
MLN008 Melanoma 62 0.174
22
P BRS047 Breast Cancer 100 0.087
23
SCK005 Sickle Cell Disease 51 0.087
24
c EST002 Estrogen-Receptor Negative Breast Cancer 42 0.087
Content
Loading form....