OBO ID: DOID:0070119
Term Name: Meckel syndrome 5 Search Ontology:
Synonyms:
  • Meckel-Gruber syndrome, type 5
  • MKS5
Definition: A Meckel syndrome that has_material_basis_in an autosomal recessive mutation of the RPGRIP1L gene on chromosome 16q12.2. https://www.ncbi.nlm.nih.gov/pubmed/17558409
References:
Ontology: Human Disease   ( DOID:0070119 )
Relationships
is a type of:
OTHER Meckel syndrome 5 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
RPGRIP1L Meckel syndrome 5 611561
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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