Disease #03925 (MKS-11 (Meckel syndrome, type 11 (MKS-11)), OMIM:615397)

Official abbreviation MKS-11
Name Meckel syndrome, type 11 (MKS-11)
OMIM ID 615397
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene TMEM231
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited N/A

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