MCID: MWT004
MIFTS: 7

Mowat-Wilson Syndrome Due to a Zeb2 Point Mutation

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

Aliases & Classifications for Mowat-Wilson Syndrome Due to a Zeb2 Point Mutation

MalaCards integrated aliases for Mowat-Wilson Syndrome Due to a Zeb2 Point Mutation:

Name: Mowat-Wilson Syndrome Due to a Zeb2 Point Mutation 59
Hirschsprung Disease and Intellectual Disability Due to a Zeb2 Point Mutation 59

Classifications:



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Orphanet 59 ORPHA261552
ICD10 via Orphanet 34 Q43.1

Summaries for Mowat-Wilson Syndrome Due to a Zeb2 Point Mutation

MalaCards based summary : Mowat-Wilson Syndrome Due to a Zeb2 Point Mutation, is also known as hirschsprung disease and intellectual disability due to a zeb2 point mutation. An important gene associated with Mowat-Wilson Syndrome Due to a Zeb2 Point Mutation is ZEB2 (Zinc Finger E-Box Binding Homeobox 2).

Related Diseases for Mowat-Wilson Syndrome Due to a Zeb2 Point Mutation

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 a Zeb2 Point Mutation

Drugs & Therapeutics for Mowat-Wilson Syndrome Due to a Zeb2 Point Mutation

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Anatomical Context for Mowat-Wilson Syndrome Due to a Zeb2 Point Mutation

Publications for Mowat-Wilson Syndrome Due to a Zeb2 Point Mutation

Variations for Mowat-Wilson Syndrome Due to a Zeb2 Point Mutation

Expression for Mowat-Wilson Syndrome Due to a Zeb2 Point Mutation

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Pathways for Mowat-Wilson Syndrome Due to a Zeb2 Point Mutation

GO Terms for Mowat-Wilson Syndrome Due to a Zeb2 Point Mutation

Sources for Mowat-Wilson Syndrome Due to a Zeb2 Point Mutation

3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
17 ExPASy
19 FMA
28 GO
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30 HGMD
31 HMDB
32 HPO
33 ICD10
34 ICD10 via Orphanet
35 ICD9CM
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46 MGI
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62 PubMed
64 QIAGEN
69 SNOMED-CT via HPO
70 SNOMED-CT via Orphanet
71 TGDB
72 Tocris
73 UMLS
74 UMLS via Orphanet
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