Disease #02377 (STWS;SJS2 (Stuve-Wiedemann syndrome (STWS; Schwartz-Jampel type 2 syndrome (SJS-2))), OMIM:601559)

Official abbreviation STWS;SJS2
Name Stuve-Wiedemann syndrome (STWS; Schwartz-Jampel type 2 syndrome (SJS-2))
OMIM ID 601559
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene LIFR
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

2 entries on 1 page. Showing entries 1 - 2.
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00132067 Pat31 PubMed: Silveira 2021, Journal: Silveira 2021 - F no Brazil - - - - - STWS;SJS2 - LIFR LIFR 1 1 Karina Silveira
00132068 2 - - F no Brazil - - - - - STWS;SJS2 - LIFR LIFR 1 1 Karina Silveira
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