MCID: PRD022
MIFTS: 11

Prader-Willi Syndrome Due to Paternal Deletion of 15q11q13 Type 1

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

Aliases & Classifications for Prader-Willi Syndrome Due to Paternal Deletion of 15q11q13 Type...

MalaCards integrated aliases for Prader-Willi Syndrome Due to Paternal Deletion of 15q11q13 Type 1:

Name: Prader-Willi Syndrome Due to Paternal Deletion of 15q11q13 Type 1 58

Classifications:

Orphanet: 58  
Rare neurological diseases
Rare infertility disorders
Rare gynaecological and obstetric diseases
Rare endocrine diseases
Developmental anomalies during embryogenesis


External Ids:

ICD10 via Orphanet 33 Q87.1
Orphanet 58 ORPHA177901

Summaries for Prader-Willi Syndrome Due to Paternal Deletion of 15q11q13 Type...

MalaCards based summary : Prader-Willi Syndrome Due to Paternal Deletion of 15q11q13 Type 1 is related to pervasive developmental disorder and autism. An important gene associated with Prader-Willi Syndrome Due to Paternal Deletion of 15q11q13 Type 1 is MAGEL2 (MAGE Family Member L2). Related phenotype is adipose tissue.

Related Diseases for Prader-Willi Syndrome Due to Paternal Deletion of 15q11q13 Type...

Diseases in the Prader-Willi Syndrome family:

Prader-Willi Syndrome Due to Paternal Deletion of 15q11q13 Type 1 Prader-Willi Syndrome Due to Paternal Deletion of 15q11q13 Type 2
Prader-Willi-Like Syndrome Due to a Point Mutation Prader-Willi Syndrome Due to Paternal 15q11q13 Deletion

Diseases related to Prader-Willi Syndrome Due to Paternal Deletion of 15q11q13 Type 1 via text searches within MalaCards or GeneCards Suite gene sharing:

(showing 8, show less)
# Related Disease Score Top Affiliating Genes
1 pervasive developmental disorder 9.7 SNRPN MAGEL2
2 autism 9.4 SNRPN NDN MAGEL2
3 autism spectrum disorder 9.4 SNRPN NDN MAGEL2
4 melanoma 9.0 OCA2 NDN MAGEL2
5 chromosomal disease 8.8 SNRPN SNORD116@ NDN MAGEL2
6 angelman syndrome 8.8 SNRPN SNORD116@ NDN MAGEL2
7 prader-willi syndrome 8.4 SNRPN SNORD116@ OCA2 NDN MAGEL2
8 prader-willi syndrome due to paternal deletion of 15q11q13 type 2 8.4 SNRPN SNORD116@ OCA2 NDN MAGEL2

Graphical network of the top 20 diseases related to Prader-Willi Syndrome Due to Paternal Deletion of 15q11q13 Type 1:



Diseases related to Prader-Willi Syndrome Due to Paternal Deletion of 15q11q13 Type 1

Symptoms & Phenotypes for Prader-Willi Syndrome Due to Paternal Deletion of 15q11q13 Type...

MGI Mouse Phenotypes related to Prader-Willi Syndrome Due to Paternal Deletion of 15q11q13 Type 1:

45 (showing 1, show less)
# Description MGI Source Accession Score Top Affiliating Genes
1 adipose tissue MP:0005375 8.8 MAGEL2 OCA2 SNRPN

Drugs & Therapeutics for Prader-Willi Syndrome Due to Paternal Deletion of 15q11q13 Type...

Search Clinical Trials , NIH Clinical Center for Prader-Willi Syndrome Due to Paternal Deletion of 15q11q13 Type 1

Genetic Tests for Prader-Willi Syndrome Due to Paternal Deletion of 15q11q13 Type...

Anatomical Context for Prader-Willi Syndrome Due to Paternal Deletion of 15q11q13 Type...

Publications for Prader-Willi Syndrome Due to Paternal Deletion of 15q11q13 Type...

Variations for Prader-Willi Syndrome Due to Paternal Deletion of 15q11q13 Type...

Expression for Prader-Willi Syndrome Due to Paternal Deletion of 15q11q13 Type...

Search GEO for disease gene expression data for Prader-Willi Syndrome Due to Paternal Deletion of 15q11q13 Type 1.

Pathways for Prader-Willi Syndrome Due to Paternal Deletion of 15q11q13 Type...

GO Terms for Prader-Willi Syndrome Due to Paternal Deletion of 15q11q13 Type...

Sources for Prader-Willi Syndrome Due to Paternal Deletion of 15q11q13 Type...

3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
17 EFO
18 ExPASy
19 FMA
28 GO
29 GTR
30 HMDB
31 HPO
32 ICD10
33 ICD10 via Orphanet
34 ICD9CM
35 IUPHAR
36 KEGG
37 LifeMap
39 LOVD
41 MedGen
43 MeSH
44 MESH via Orphanet
45 MGI
48 NCI
49 NCIt
50 NDF-RT
53 NINDS
54 Novoseek
56 OMIM
57 OMIM via Orphanet
61 PubMed
63 QIAGEN
68 SNOMED-CT via HPO
69 TGDB
70 Tocris
71 UMLS
72 UMLS via Orphanet
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