OBO ID: DOID:0110709
Term Name: hypotrichosis 12 Search Ontology:
Synonyms:
  • Hypt12
Definition: A hypotrichosis that has_material_basis_in a autosomal dominant mutation of the RPL21 gene on chromosome 13q12.2. https://www.ncbi.nlm.nih.gov/pubmed/21412954
References:
Ontology: Human Disease   ( DOID:0110709 )
Relationships
is a type of:
OTHER hypotrichosis 12 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
RPL21 Hypotrichosis 12 615885
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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