MCID: PRD025
MIFTS: 12

Prader-Willi Syndrome Due to Imprinting Mutation

Categories: Genetic diseases, Rare diseases, Neuronal diseases, Reproductive diseases, Endocrine diseases, Fetal 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 translocation and prader-willi syndrome due to maternal uniparental disomy of chromosome 15. 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

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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
16 ExPASy
18 FMA
27 GO
28 GTR
29 HGMD
30 HMDB
31 HPO
32 ICD10
33 ICD10 via Orphanet
34 ICD9CM
35 IUPHAR
36 KEGG
37 LifeMap
39 MedGen
41 MeSH
42 MESH via Orphanet
43 MGI
45 NCI
46 NCIt
47 NDF-RT
50 NINDS
51 Novoseek
53 OMIM
54 OMIM via Orphanet
58 PubMed
60 QIAGEN
65 SNOMED-CT via HPO
66 SNOMED-CT via Orphanet
67 TGDB
68 Tocris
69 UMLS
70 UMLS via Orphanet
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