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

Official abbreviation MKS10;JBTS34
Name syndrome, Meckel, type 10 (MKS10, incl. Joubert syndrome 3434)
OMIM ID 614175
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene B9D2
Associated tissues -
Disease features -
Remarks -