MCID: PRD027
MIFTS: 5

Prader-Willi Syndrome Due to Paternal 15q11q13 Deletion

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

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

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

MalaCards based summary : Prader-Willi Syndrome Due to Paternal 15q11q13 Deletion

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

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

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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