ZFIN Human Disease: autosomal dominant Alport syndrome

OBO ID: DOID:0110032

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:	GARD:624 OMIM:104200 ORDO:88918
Ontology:	Human Disease ( DOID:0110032 )

Relationships

is a type of:	Alport syndrome autosomal dominant disease Alport syndrome autosomal dominant disease Show first 5 Terms

OTHER autosomal dominant Alport syndrome PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
COL4A3	col4a3	Alport syndrome 3A, autosomal dominant	104200

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None