OBO ID: DOID:0070122
Term Name: Meckel syndrome 8 Search Ontology:
Synonyms:
  • Meckel-Gruber syndrome, type 8
  • MKS8
Definition: A Meckel syndrome that has_material_basis_in an autosomal recessive mutation of the TCTN2 gene on chromosome 12q24.31. https://www.ncbi.nlm.nih.gov/pubmed/21462283
References:
Ontology: Human Disease   ( DOID:0070122 )
Relationships
is a type of:
OTHER Meckel syndrome 8 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
TCTN2 ?Meckel syndrome 8 613885
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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