MCID: PRD042
MIFTS: 7

Prader-Willi-Like Syndrome Due to a Point Mutation

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

Aliases & Classifications for Prader-Willi-Like Syndrome Due to a Point Mutation

Summaries for Prader-Willi-Like Syndrome Due to a Point Mutation

MalaCards based summary : Prader-Willi-Like Syndrome Due to a Point Mutation, is also known as pws-like due to a point mutation. An important gene associated with Prader-Willi-Like Syndrome Due to a Point Mutation is SIM1 (SIM BHLH Transcription Factor 1).

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Symptoms & Phenotypes for Prader-Willi-Like Syndrome Due to a Point Mutation

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Expression for Prader-Willi-Like Syndrome Due to a Point Mutation

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Pathways for Prader-Willi-Like Syndrome Due to a Point Mutation

GO Terms for Prader-Willi-Like Syndrome Due to a Point Mutation

Sources for Prader-Willi-Like Syndrome Due to a Point Mutation

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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