OBO ID: DOID:0110032
Term Name: autosomal dominant Alport syndrome Search Ontology:
Synonyms:
Definition: An Alport syndrome that has_material_basis_in heterozygous mutation in the COL4A3 gene. https://www.ncbi.nlm.nih.gov/pubmed/11044206
References:
Ontology: Human Disease   (DOID:0110032)
OTHER autosomal dominant Alport syndrome PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
COL4A3 Alport syndrome 3, autosomal dominant 104200
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None