Search Ontology:
Human Disease

Meckel syndrome 8

Term ID
DOID:0070122
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 Pages
Alliance (1)
Genes Involved
Zebrafish Models
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