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DOID:0080519 - PAPA syndrome
Disease Ontology Definition:A syndrome that is characterised by pyoderma gangrenosum, pyogenic arthritis, acne and suppurative hidradenitis and heterozygous mutation in the PSTPIP1 gene on chromosome 15q24.
Synonyms: pyogenic arthritis, pyoderma gangrenosum and acne,
Echinobase Genes :
MIM:604416 - pyogenic sterile arthritis, pyoderma gangrenosum, and acne |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
autosomal dominant disease (is_a),
syndrome (is_a)