Search Ontology:
Human Disease
erythrokeratodermia variabilis et progressiva 5
- Term ID
- DOID:0080251
- Synonyms
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- Definition
- An erythrokeratodermia variabilis that has_material_basis_in homozygous mutation in the KRT83 gene on chromosome 12q13. https://pubmed.ncbi.nlm.nih.gov/27965375/
- References
- Ontology
- Human Disease ( DOID:0080251 )
- is a type of
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Genes Involved
Zebrafish Models