Disease #00229 (PWS (Prader-Willi syndrome (PWS)), OMIM:176270)

Official abbreviation PWS
Name Prader-Willi syndrome (PWS)
OMIM ID 176270
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 2
Phenotype entries for this disease 3
Associated with 2 genes NDN, SNRPN
Associated tissues -
Disease features -
Remarks -
Date created 2013-10-09 19:21:42 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00305399 130504 - - M ? Germany - - - - - PWS Makrosomie, Adipositas TMEM43 TMEM43 1 1 Andreas Laner
00472238 - Verebi et al. (submitted) - F - France - - - - - PWS 0001511: Intrauterine growth retardation, 001531: Growth retardation in infants, 0001319: Neonatal hypotonia, 0001290: Generalised hypotonia, 0008872: Eating disorders in children - UBE3A 1 1 Camille Verebi
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