OBO ID: DOID:0070121
Term Name: Meckel syndrome 7 Search Ontology:
Synonyms:
  • Meckel-Gruber syndrome, type 7
  • MKS7
Definition: A Meckel syndrome that has_material_basis_in an autosomal recessive mutation of the NPHP3 gene on chromosome 3q22.1. https://www.ncbi.nlm.nih.gov/pubmed/18371931
References:
Ontology: Human Disease   ( DOID:0070121 )
Relationships
is a type of:
OTHER Meckel syndrome 7 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
NPHP3 Meckel syndrome 7 267010
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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