Search Ontology:
Human Disease

primary pigmented nodular adrenocortical disease 2

Term ID
DOID:0070547
Synonyms
  • PPNAD2
Definition
A primary pigmented nodular adrenocortical disease that has_material_basis_in heterozygous mutation in the PDE11A gene on chromosome 2q31.2. https://pubmed.ncbi.nlm.nih.gov/16767104/
References
Ontology
Human Disease   ( DOID:0070547 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models