OBO ID: DOID:0070115
Term Name: Meckel syndrome 1 Search Ontology:
Synonyms:
  • Meckel-Gruber syndrome, type 1
  • MKS1
Definition: A Meckel syndrome that has_material_basis_in an autosomal recessive mutation of the MKS1 gene on chromosome 17q22. https://www.ncbi.nlm.nih.gov/pubmed/16415886
References:
Ontology: Human Disease   ( DOID:0070115 )
Relationships
is a type of:
OTHER Meckel syndrome 1 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
MKS1 Meckel syndrome 1 249000
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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