Oculocutaneous Albinism (OCA)

Alias:
Albinism, Oculocutaneous
Oca
Oca - [oculocutaneous Albinism]
Albinism Oculocutaneous
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Oculocutaneous Albinism, also known as albinism, oculocutaneous, is related to albinism, oculocutaneous, type ia and albinism, oculocutaneous, type vi. An important gene associated with Oculocutaneous Albinism is OCA2 (OCA2 Melanosomal Transmembrane Protein), and among its related pathways/superpathways are Regulation of expression of SLITs and ROBOs and Prader-Willi and Angelman syndrome. The drugs Pirfenidone and Nitisinone have been mentioned in the context of this disorder. Affiliated tissues include skin and eye, and related phenotypes are pigmentation and homeostasis/metabolism
Related ID:
MESH:D016115
ICD11:1189424097

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Newborn
1-9/100000
38
759
62

Medical Symptom

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

Gene & Mutation

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Gene
Function
Score
Mutations
No data available

Related Drugs

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CAS Number
Status
Phase
No data available

Disease Model

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

References Literature

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PMID
Journal
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IF
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