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Human Disease

Meckel syndrome 3

Term ID
DOID:0070117
Synonyms
  • Meckel-Gruber syndrome, type 3
  • MKS3
Definition
A Meckel syndrome that has_material_basis_in an autosomal recessive mutation of the TMEM67 gene on chromosome 8q22.1. https://www.ncbi.nlm.nih.gov/pubmed/16415887
References
Ontology
Human Disease   ( DOID:0070117 )
Relationships
is a type of
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Genes Involved
Zebrafish Models