OBO ID: DOID:0070120
Term Name: Meckel syndrome 6 Search Ontology:
Synonyms:
  • Meckel-Gruber syndrome, type 6
  • MKS6
Definition: A Meckel syndrome that has_material_basis_in an autosomal recessive mutation of CC2D2A on chromosome 4p15.32.https://www.ncbi.nlm.nih.gov/pubmed/18513680
References:
Ontology: Human Disease   (DOID:0070120)
Relationships
is a type of:
OTHER Meckel syndrome 6 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
CC2D2A Meckel syndrome 6 612284
ZEBRAFISH MODELSNo data available
PHENOTYPE No data available

CITATIONS: None