Search Ontology:
Human Disease

erythrokeratodermia variabilis et progressiva 5

Term ID
DOID:0080251
Synonyms
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 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models