Meckel syndrome 12

Term ID

DOID:0061297

Synonyms

Definition

A Meckel syndrome that has_material_basis_in a compound heterozygous mutation in the KIF14 gene on chromosome 1q31. https://pubmed.ncbi.nlm.nih.gov/24128419/

References

• MIM:616258

Ontology

Human Disease   ( DOID:0061297 )