MCID: PRD024
MIFTS: 6

Prader-Willi Syndrome Due to Translocation

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

Symptoms & Phenotypes for Prader-Willi Syndrome Due to Translocation

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Expression for Prader-Willi Syndrome Due to Translocation

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

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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
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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