Disease #01021 (MKS10;JBTS34 (Meckel syndrome, type 10 (MKS10, incl. Joubert syndrome 3434)), OMIM:614175)

Official abbreviation MKS10;JBTS34
Name Meckel syndrome, type 10 (MKS10, incl. Joubert syndrome 3434)
OMIM ID 614175
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene B9D2
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)

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