Search Ontology:
Human Disease

nephronophthisis 19

Term ID
DOID:0111126
Synonyms
  • NPHP19
Definition
A nephronophthisis that has_material_basis_in homozygous or compound heterozygous mutation in the DCDC2 gene on chromosome 6p22. https://www.ncbi.nlm.nih.gov/pubmed/25557784
References
Ontology
Human Disease   ( DOID:0111126 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
Citations
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