OBO ID: DOID:0110708
Term Name: hypotrichosis 11 Search Ontology:
Synonyms:
  • Hypt11
Definition: A hypotrichosis that has_material_basis_in a autosomal dominant mutation of the SNRPE gene on chromosome 1q32.1. https://www.ncbi.nlm.nih.gov/pubmed/23246290
References:
Ontology: Human Disease   ( DOID:0110708 )
Relationships
is a type of:
OTHER hypotrichosis 11 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
SNRPE Hypotrichosis 11 615059
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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