MCID: PRD024
MIFTS: 10

Prader-Willi Syndrome Due to Translocation

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

Aliases & Classifications for Prader-Willi Syndrome Due to Translocation

Summaries for Prader-Willi Syndrome Due to Translocation

MalaCards based summary : Prader-Willi Syndrome Due to Translocation is related to prader-willi syndrome due to imprinting mutation and prader-willi syndrome due to paternal deletion of 15q11q13 type 1. An important gene associated with Prader-Willi Syndrome Due to Translocation is SNRPN (Small Nuclear Ribonucleoprotein Polypeptide N).

Related Diseases for Prader-Willi Syndrome Due to Translocation

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



Diseases related to Prader-Willi Syndrome Due to Translocation

Symptoms & Phenotypes for Prader-Willi Syndrome Due to Translocation

Drugs & Therapeutics for Prader-Willi Syndrome Due to Translocation

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Genetic Tests for Prader-Willi Syndrome Due to Translocation

Anatomical Context for Prader-Willi Syndrome Due to Translocation

Publications for Prader-Willi Syndrome Due to Translocation

Variations for Prader-Willi Syndrome Due to Translocation

Expression for Prader-Willi Syndrome Due to Translocation

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

Pathways for Prader-Willi Syndrome Due to Translocation

GO Terms for Prader-Willi Syndrome Due to Translocation

Sources for Prader-Willi Syndrome Due to Translocation

3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
16 ExPASy
18 FMA
27 GO
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30 HMDB
31 HPO
32 ICD10
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65 SNOMED-CT via HPO
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67 TGDB
68 Tocris
69 UMLS
70 UMLS via Orphanet
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