Disease #00081 (MKS-6 (Meckel syndrome, type 6 (MKS-6)), OMIM:612284)

Official abbreviation MKS-6
Name Meckel syndrome, type 6 (MKS-6)
OMIM ID 612284
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene CC2D2A
Associated tissues -
Disease features -
Remarks -
Date created 2012-11-09 15:23:18 +01:00 (CET)
Date last edited N/A

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