Disease #04623 (HJS2;MRD36 (Houge-Janssens syndrome, type 2), OMIM:616362)

Official abbreviation HJS2;MRD36
Name Houge-Janssens syndrome, type 2
OMIM ID 616362
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene PPP2R1A
Associated tissues -
Disease features -
Remarks -
Date created 2015-09-23 10:25:23 +02:00 (CEST)
Date last edited 2025-03-18 19:44:50 +01:00 (CET)

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