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Cancer, Alopecia, Pigment Dyscrasia, Onychodystrophy, and Keratoderma (CAPOK)

Alias:
Capok
Pigmentation Defects-Palmoplantar Keratoderma-Skin Carcinoma Syndrome
Capok Syndrome
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Cancer, Alopecia, Pigment Dyscrasia, Onychodystrophy, and Keratoderma, is also known as capok. An important gene associated with Cancer, Alopecia, Pigment Dyscrasia, Onychodystrophy, and Keratoderma is SASH1 (SAM And SH3 Domain Containing 1). Affiliated tissues include skin, and related phenotypes are alopecia and hypermelanotic macule
Related ID：
MALACARDS：CNC020
OMIM：618373
MESH：D007039

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Infant
<1/1000000
1
6
1
CNC020

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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