Search Ontology:
Human Disease

hypotrichosis 11

Term ID
DOID:0110708
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 Pages
Alliance (1)
Genes Involved
Zebrafish Models
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