Meckel syndrome 10

Term ID

DOID:0061295

Synonyms

Definition

A Meckel syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the B9D2 gene on chromosome 19q13. https://pubmed.ncbi.nlm.nih.gov/31411728/

References

• MIM:614175

Ontology

Human Disease   ( DOID:0061295 )