Disease #00078 (MKS-1 (Meckel syndrome, type 1 (MKS-1, Meckel-Gruber syndrome)), OMIM:249000)

Official abbreviation MKS-1
Name Meckel syndrome, type 1 (MKS-1, Meckel-Gruber syndrome)
OMIM ID 249000
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene MKS1
Associated tissues -
Disease features -
Remarks -
Date created 2012-11-09 15:11:48 +01:00 (CET)
Date last edited N/A

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