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DOID:0070547 - primary pigmented nodular adrenocortical disease 2
Disease Ontology Definition:A primary pigmented nodular adrenocortical disease that has_material_basis_in heterozygous mutation in the PDE11A gene on chromosome 2q31.2.
Synonyms: PPNAD2,
Xenbase Genes :
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
autosomal dominant disease (is_a),
primary pigmented nodular adrenocortical disease (is_a)