Visualize Submit Comment
Metadata
ID DOID:0050658
Name Bart-Pumphrey syndrome
Definition A syndrome that is characterized by leukonychia, wart-like skin growths, palmoplantar keratoderma and hearing loss, has_material_basis_in heterozygous mutation in the GJB2 gene on chromosome 13q12.
https://ghr.nlm.nih.gov/condition/bart-pumphrey-syndrome
Xrefs

OMIM:149200

Synonyms

KNUCKLE PADS, LEUKONYCHIA, AND SENSORINEURAL DEAFNESS [EXACT]

Parent Relationships

is_a syndrome

is_a autosomal dominant disease

Add an item to the term tracker