MCID: PRD023
MIFTS: 12

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

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

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

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 angelman syndrome and autism. An important gene associated with Prader-Willi Syndrome Due to Paternal Deletion of 15q11q13 Type 2 is SNORD116@ (Small Nucleolar RNA, C/D Box 116 Cluster). 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:

46
# 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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Anatomical Context for Prader-Willi Syndrome Due to Paternal Deletion of 15q11q13 Type...

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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 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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