Disease #00067 (KURIS (KURY-ISIDOR SYNDROME), OMIM:619762)

Official abbreviation KURIS
Name KURY-ISIDOR SYNDROME
OMIM ID 619762
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene BAP1
Associated tissues -
Disease features -
Remarks -

  Powered by LOVD v.3.0 Build 29
LOVD software ©2004-2023 Leiden University Medical Center 		There are currently no updates.