Disease #03900 (CPPB2 (precocious puberty, central, type 2 (CPPB-2)), OMIM:615346)

Official abbreviation CPPB2
Name precocious puberty, central, type 2 (CPPB-2)
OMIM ID 615346
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 3
Phenotype entries for this disease 2
Associated with 1 gene MKRN3
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)


Individuals

3 entries on 1 page. Showing entries 1 - 3.
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00038513 - - - F - Belgium - - - - - CPPB2 - MKRN3 MKRN3 1 1 Cecile Libioulle
00229577 - PubMed: Yakoreva 2019, Journal: Yakoreva 2019 extended family, 4 affected, all variant on paternal alelle F - Estonia - - - - - CPPB2 - - MKRN3 1 4 Sander Pajusalu
00432294 214326 - - F ? - - - - - - CPPB2, KBGS Generalized non-motor (absence) seizure, Neurodevelopmental delay, Precocious puberty ANKRD11, MKRN3 ANKRD11, MKRN3 2 1 Andreas Laner
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