OBO ID: DOID:0070116
Term Name: Meckel syndrome 2 Search Ontology:
Synonyms:
  • Meckel-Gruber syndrome, type 2
  • MKS2
Definition: A Meckel syndrome that has_material_basis_in an autosomal recessive mutation of TMEM216 on chromosome 11q12.2. https://www.ncbi.nlm.nih.gov/pubmed/20512146
References:
Ontology: Human Disease   (DOID:0070116)
OTHER Meckel syndrome 2 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
TMEM216 Meckel syndrome 2 603194
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None