MCID: MWT002
MIFTS: 9

Mowat-Wilson Syndrome Due to Monosomy 2q22

Categories: Neuronal diseases, Fetal diseases, Rare diseases, Genetic diseases, Mental diseases

Aliases & Classifications for Mowat-Wilson Syndrome Due to Monosomy 2q22

MalaCards integrated aliases for Mowat-Wilson Syndrome Due to Monosomy 2q22:

Name: Mowat-Wilson Syndrome Due to Monosomy 2q22 59
Hirschsprung Disease and Intellectual Disability Due to 2q22 Microdeletion 59
Hirschsprung Disease and Intellectual Disability Due to Monosomy 2q22 59
Hirschsprung Disease and Intellectual Disability Due to Del(2)(q22) 59
Mowat-Wilson Syndrome Due to 2q22 Microdeletion 59
Mowat-Wilson Syndrome Due to Del(2)q(22) 59

Classifications:



External Ids:

Orphanet 59 ORPHA261537
ICD10 via Orphanet 34 Q43.1

Summaries for Mowat-Wilson Syndrome Due to Monosomy 2q22

MalaCards based summary : Mowat-Wilson Syndrome Due to Monosomy 2q22, is also known as hirschsprung disease and intellectual disability due to 2q22 microdeletion. An important gene associated with Mowat-Wilson Syndrome Due to Monosomy 2q22 is ZEB2 (Zinc Finger E-Box Binding Homeobox 2).

Related Diseases for Mowat-Wilson Syndrome Due to Monosomy 2q22

Diseases in the Mowat-Wilson Syndrome family:

Mowat-Wilson Syndrome Due to Monosomy 2q22 Mowat-Wilson Syndrome Due to a Zeb2 Point Mutation

Symptoms & Phenotypes for Mowat-Wilson Syndrome Due to Monosomy 2q22

Drugs & Therapeutics for Mowat-Wilson Syndrome Due to Monosomy 2q22

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Expression for Mowat-Wilson Syndrome Due to Monosomy 2q22

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GO Terms for Mowat-Wilson Syndrome Due to Monosomy 2q22

Sources for Mowat-Wilson Syndrome Due to Monosomy 2q22

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