Disease #00095 (MWS (Mowat-Wilson Syndrome), OMIM:235730)

Official abbreviation MWS
Name Mowat-Wilson Syndrome
OMIM ID 235730
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene ZEB2
Associated tissues -
Disease features -
Remarks -


Individuals

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00000550 S Balasubramaniam et al.(2010) F Malaysia Chinese - - - MWS Growth parameters below the 3rd percentile, had sparse, coarse hair, medially flared thick eyebrows, hypertelorism, a saddle nose, epicanthic folds, a pair of prominent simple ears with uplifted ear lobes, long tapered fingers and a prominent pointed chin, severe constipation during the neonatal period, hypotonic, globally delayed and dysmorphic. ZEB2 ZEB2 1 1 Nur Aisyah Athirah
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