MCID: PRD027
MIFTS: 5

Prader-Willi Syndrome Due to Paternal 15q11q13 Deletion

Categories: Neuronal diseases, Reproductive diseases, Endocrine diseases, Fetal diseases, Rare diseases, Genetic 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
16 ExPASy
18 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 MedGen
42 MeSH
43 MESH via Orphanet
44 MGI
46 NCI
47 NCIt
48 NDF-RT
51 NINDS
52 Novoseek
54 OMIM
55 OMIM via Orphanet
59 PubMed
60 QIAGEN
65 SNOMED-CT via HPO
66 SNOMED-CT via Orphanet
67 TGDB
68 Tocris
69 UMLS
70 UMLS via Orphanet
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