MCID: PRD023
MIFTS: 13

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

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 phenotypes are adipose tissue and behavior/neurological

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:

47
# Description MGI Source Accession Score Top Affiliating Genes
1 adipose tissue MP:0005375 9.13 MAGEL2 OCA2 SNRPN
2 behavior/neurological MP:0005386 8.92 MAGEL2 NDN OCA2 SNRPN

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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 EFO
18 ExPASy
20 FMA
29 GO
30 GTR
31 HGMD
32 HMDB
33 HPO
34 ICD10
35 ICD10 via Orphanet
36 ICD9CM
37 IUPHAR
38 KEGG
39 LifeMap
41 LOVD
43 MedGen
45 MeSH
46 MESH via Orphanet
47 MGI
50 NCI
51 NCIt
52 NDF-RT
55 NINDS
56 Novoseek
58 OMIM
59 OMIM via Orphanet
63 PubMed
65 QIAGEN
70 SNOMED-CT via HPO
71 SNOMED-CT via Orphanet
72 TGDB
73 Tocris
74 UMLS
75 UMLS via Orphanet
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