Disease #00568 (MOWS (Mowat-Wilson syndrome), OMIM:235730)

Official abbreviation MOWS
Name Mowat-Wilson syndrome
OMIM ID 235730
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene ZEB2
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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00081000 - PubMed: Trujillano 2017 unaffected non-carrier parents - - - - - - - - MOWS Mowat-Wilson syndrome (OMIM:235730) ZEB2 ZEB2 1 1 Daniel Trujillano
00449560 290575 - - F no Turkey - - - - - MOWS Neurodevelopmental delay, Ventricular septal defect, Patent ductus arteriosus, Complex febrile seizure, Microcephaly, Delayed speech and language development, Hypertelorism, Abnormality of the face, Delayed gross motor development ZEB2 ZEB2 1 1 Andreas Laner
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