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Birt-Hogg-Dube syndrome

Disease Summary
Associated Targets (3)
Tbio

3


GARD Rare
Mondo Description Birt-Hogg-Dube (BHD) syndrome is characterized by skin lesions, kidney tumors, and pulmonary cysts that may be associated with pneumothorax. It is a rare clinicopathologic condition named after the three Canadian physicians who reported the syndrome in 1977.
Uniprot Description A rare autosomal dominant genodermatosis characterized by hair follicle hamartomas (fibrofolliculomas), kidney tumors, and spontaneous pneumothorax. Fibrofolliculomas are part of the triad of Birt-Hogg-Dube syndrome skin lesions that also includes trichodiscomas and acrochordons. Onset of this dermatologic condition is invariably in adulthood. Birt-Hogg-Dube syndrome is associated with a variety of histologic types of renal tumors, including chromophobe renal cell carcinoma (RCC), benign renal oncocytoma, clear-cell RCC and papillary type I RCC. Multiple lipomas, angiolipomas, and parathyroid adenomas are also seen in Birt-Hogg-Dube syndrome patients.
Disease Ontology Description An autosomal dominant disease that is characterized by the development of skin papules on the head, face and upper torso, has_material_basis_in heterozygous mutation in the gene encoding folliculin on chromosome 17p11.
Mondo Term and Equivalent IDs
MONDO:0007607:  Birt-Hogg-Dube syndrome
EFO:1001273: 
GARD:0002322: 
MESH:D058249: 
NCIT:C28244: 
Orphanet:122: 
SCTID:110985001: 
UMLS:C0346010: