MCID: PRD025
MIFTS: 11

Prader-Willi Syndrome Due to Imprinting Mutation

Categories: Neuronal diseases, Reproductive diseases, Endocrine diseases, Fetal diseases, Rare diseases, Genetic diseases

Aliases & Classifications for Prader-Willi Syndrome Due to Imprinting Mutation

Summaries for Prader-Willi Syndrome Due to Imprinting Mutation

MalaCards based summary : Prader-Willi Syndrome Due to Imprinting Mutation is related to prader-willi syndrome due to maternal uniparental disomy of chromosome 15 and angelman syndrome. An important gene associated with Prader-Willi Syndrome Due to Imprinting Mutation is SNRPN (Small Nuclear Ribonucleoprotein Polypeptide N).

Related Diseases for Prader-Willi Syndrome Due to Imprinting Mutation

Graphical network of the top 20 diseases related to Prader-Willi Syndrome Due to Imprinting Mutation:



Diseases related to Prader-Willi Syndrome Due to Imprinting Mutation

Symptoms & Phenotypes for Prader-Willi Syndrome Due to Imprinting Mutation

Drugs & Therapeutics for Prader-Willi Syndrome Due to Imprinting Mutation

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Anatomical Context for Prader-Willi Syndrome Due to Imprinting Mutation

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Variations for Prader-Willi Syndrome Due to Imprinting Mutation

Expression for Prader-Willi Syndrome Due to Imprinting Mutation

Search GEO for disease gene expression data for Prader-Willi Syndrome Due to Imprinting Mutation.

Pathways for Prader-Willi Syndrome Due to Imprinting Mutation

GO Terms for Prader-Willi Syndrome Due to Imprinting Mutation

Sources for Prader-Willi Syndrome Due to Imprinting Mutation

3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
17 ExPASy
19 FMA
28 GO
29 GTR
30 HGMD
31 HMDB
32 HPO
33 ICD10
34 ICD10 via Orphanet
35 ICD9CM
36 IUPHAR
37 KEGG
38 LifeMap
40 LOVD
42 MedGen
44 MeSH
45 MESH via Orphanet
46 MGI
49 NCI
50 NCIt
51 NDF-RT
54 NINDS
55 Novoseek
57 OMIM
58 OMIM via Orphanet
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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