Disease #06869 (WRWFFR (Wieacker-Wolff syndrome, female-restricted), OMIM:301041)

Official abbreviation WRWFFR
Name Wieacker-Wolff syndrome, female-restricted
OMIM ID 301041
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 ZC4H2
Associated tissues -
Disease features -
Remarks -
Date created 2021-12-10 23:20:41 +01:00 (CET)
Date last edited N/A


Individuals

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00466380 - Pending - F - France - - - - - WRWFFR Arthrogryposis multiplex congenita - ZC4H2 1 1 Camille Verebi
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