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 the CC2D2A gene 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 MODELS No data available
PHENOTYPE No data available

CITATIONS: None
Your Input Welcome
We welcome your input and comments. Please use this form to recommend updates to the information in ZFIN. We appreciate as much detail as possible and references as appropriate. We will review your comments promptly.
Please check the highlighted fields and try again.
Thank you for submitting comments. Your input has been emailed to ZFIN curators who may contact you if additional information is required.
Oops. Something went wrong. Please try again later.