OBO ID: DOID:0080273
Term Name: polycystic kidney disease 5 Search Ontology:
Synonyms:
Definition: A autosomal recessive polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of homozygous mutation in the DZIP1L gene on chromosome 3q22. https://www.omim.org/entry/617610
References:
Ontology: Human Disease   ( DOID:0080273 )
Relationships
is a type of:
OTHER polycystic kidney disease 5 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
DZIP1L Polycystic kidney disease 5 617610
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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