Search Ontology:
Human Disease

Meckel syndrome 14

Term ID
DOID:0070703
Synonyms
  • MKS14
Definition
A Meckel syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the TXNDC15 gene on chromosome 5q31. (2)
References
Ontology
Human Disease   ( DOID:0070703 )
Relationships
Other Pages
Genes Involved
Zebrafish Models
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