Search Ontology:
Human Disease
peeling skin syndrome 3
- Term ID
- DOID:0070522
- Synonyms
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- peeling skin syndrome type A
- PSS3
- Definition
- A peeling skin syndrome that has_material_basis_in homozygous mutation in the CHST8 gene on chromosome 19q13.11. https://pubmed.ncbi.nlm.nih.gov/22289416/
- References
- Ontology
- Human Disease ( DOID:0070522 )
- is a type of
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