Disease #07056 (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 1
Phenotype entries for this disease 1
Associated with 1 gene BAP1
Associated tissues -
Disease features -
Remarks -
Date created 2023-12-24 13:30:59 +01:00 (CET)
Date last edited N/A


Individuals

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00465592 329845 - - M no Germany - - - - - KURIS Neurodevelopmental delay, Polycythemia, Hearing impairment, Lymphangioma BAP1 BAP1 1 1 Andreas Laner
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