Search Ontology:
Human Disease

hypotrichosis 15

Term ID
DOID:0060968
Synonyms
Definition
A hypotrichosis that is characterized by sparse or absent hair on the scalp and/or body, and eyebrows and eyelashes may be sparse or absent as well that has_material_basis_in homozygous mutation in the C3ORF52 gene on chromosome 3q13. https://pubmed.ncbi.nlm.nih.gov/32336749/
References
Ontology
Human Disease   ( DOID:0060968 )
Relationships
is a type of
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Genes Involved
Zebrafish Models