OBO ID: DOID:0070117
Term Name: Meckel syndrome 3 Search Ontology:
Synonyms:
  • Meckel-Gruber syndrome, type 3
  • MKS3
Definition: A Meckel syndrome that has_material_basis_in an autosomal recessive mutation of the TMEM67 gene on chromosome 8q22.1. https://www.ncbi.nlm.nih.gov/pubmed/16415887
References:
Ontology: Human Disease   ( DOID:0070117 )
Relationships
is a type of:
OTHER Meckel syndrome 3 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
TMEM67 Meckel syndrome 3 607361
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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