Albinism, Oculocutaneous, Type Ib (OCA1B)

Alias:
Oca1b
Oculocutaneous Albinism Type 1b
Oculocutaneous Albinism Type Ib
Albinism, Yellow Mutant Type
Temperature-Sensitive Oculocutaneous Albinism Type 1
Oculocutaneous Albinism, Amish Type
Platinum Oculocutaneous Albinism
Yellow Oculocutaneous Albinism
Yellow Albinism
Albinism, Oculocutaneous, Type I, Temperature-Sensitive
Oculocutaneous Albinism Type I Temperature-Sensitive
Minimal Pigment Oculocutaneous Albinism
Oculocutaneous Albinism, Type Ib
Albinism, Oculocutaneous, 1b
Albinism Yellow Mutant Type
Ts Oca Type 1
Oca1-Ts
Oca-Its
Oca-Ib
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基础信息
疾病表征
基因 & 突变
靶点药物
疾病模型
文献报道
白化病,皮肤和眼睛,类型IB,也称为oca1b,与白化病,皮肤和眼睛,类型IA和皮肤和眼睛白化病有关。与白化病,皮肤和眼睛,类型IB有关的重要基因是TYR(酪氨酸酶),其相关通路/超级通路包括SLITs和ROBOs表达的调节以及Prader-Willi和天使综合症。在该疾病的背景下提到了尼替尼和酶抑制剂。附属组织包括皮肤和眼睛,相关表型为视网膜色素沉着异常和斜视。
Related ID:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常隐
新生儿
1-9/100000
10
386
43

Medical Symptom

#
Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

#
Gene
Function
Score
Mutations
No data available

Related Drugs

Name
CAS Number
Status
Phase
No data available

Disease Model

Category
Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

Title
PMID
Journal
Year
IF
No Data Found!
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