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Metadata
ID DOID:0070120
Name Meckel syndrome 6
Definition A Meckel syndrome that has_material_basis_in an autosomal recessive mutation of the CC2D2A gene on chromosome 4p15.32.
https://www.ncbi.nlm.nih.gov/pubmed/18513680
Xrefs

ICD10CM:Q61.9

OMIM:612284

Synonyms

Meckel-Gruber syndrome, type 6 [EXACT]

MKS6 [EXACT]

Parent Relationships

is_a Meckel syndrome

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