MCID: PRD023
MIFTS: 11

Prader-Willi Syndrome Due to Paternal Deletion of 15q11q13 Type 2

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 2:

Name: Prader-Willi Syndrome Due to Paternal Deletion of 15q11q13 Type 2 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 ORPHA177904

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 2 is related to cryptorchidism, unilateral or bilateral and strabismus. An important gene associated with Prader-Willi Syndrome Due to Paternal Deletion of 15q11q13 Type 2 is MAGEL2 (MAGE Family Member L2). Related phenotype is adipose tissue.

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

Graphical network of the top 20 diseases related to Prader-Willi Syndrome Due to Paternal Deletion of 15q11q13 Type 2:



Diseases related to Prader-Willi Syndrome Due to Paternal Deletion of 15q11q13 Type 2

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 2:

45
# 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...

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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 2.

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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