Visualize Submit Comment
Metadata
ID DOID:0070117
Name Meckel syndrome 3
Definition A Meckel syndrome that has_material_basis_in an autosomal recessive mutation of TMEM67 on chromosome 8q22.1.
https://www.ncbi.nlm.nih.gov/pubmed/16415887
Xrefs

ICD10CM:Q61.9

OMIM:607361

Synonyms

Meckel-Gruber syndrome, type 3 [EXACT]

MKS3 [EXACT]

Parent Relationships

is_a Meckel syndrome

Add an item to the term tracker