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English: Mowat–Wilson syndrome is a rare genetic disorder that was clinically delineated by Dr. D. R. Mowat and Dr. M. J. Wilson in 1998.
Español: El síndrome de Mowat Wilson es una enfermedad genética rara que fue descrita clínicamente por los doctores D. R. Mowat y Dr. M. J. Wilson en 1998.
Mowat-Wilson syndrome 
rare genetic disorder
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Instance of disease,
developmental defect during embryogenesis
Subclass of syndrome,
Hirschsprung's disease,
multiple congenital anomalies/dysmorphic syndrome-intellectual disability,
syndromic intestinal malformation,
genetic syndromic intellectual disability,
genetic disease
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sindrome di Mowat-Wilson (it); Mowat–Wilson-szindróma (hu); Zespół Mowata-Wilsona (pl); Mowat-Wilson syndrome (nl); Mowat-Wilson-Syndrom (de); Mowat–Wilson syndrome (en-gb); Mowat-Wilson syndrome (en); Mowat–Wilson syndrome (en-ca); Síndrome de Mowat-Wilson (es); Syndrome de Mowat-Wilson (fr) enfermedad humana (es); Krankheit (de); rare genetic disorder (en); مرض يصيب الإنسان (ar); malattia genetica rara (it) Síndrome de Mowat Wilson, Sindrome de Mowat-Wilson, Sindrome de Mowat Wilson (es); Zespół Mowata i Wilsona (pl); Hirschsprung disease mental retardation syndrome, microcephaly, mental retardation, and distinct facial featrues, with or without Hirschprung disease, MOWAT-WILSON SYNDROME; MOWS, Hirschsprung Disease-Mental Retardation Syndrome, MOWAT-WILSON SYNDROME, MOWS, Mental retardation, microcephaly, and distinct facial features with or without Hirschsprung disease, Microcephaly, Mental Retardation, and Distinct Facial Features, With or Without Hirschsprung Disease, Hirschsprung disease-intellectual disability syndrome (en)

Media in category "Mowat–Wilson syndrome"

The following 3 files are in this category, out of 3 total.