MCID: PRD034
MIFTS: 7

Prader-Willi-Like Syndrome Due to Point Mutation

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

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

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

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

Related Diseases for Prader-Willi-Like Syndrome Due to Point Mutation

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

Drugs & Therapeutics for Prader-Willi-Like Syndrome Due to Point Mutation

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Anatomical Context for Prader-Willi-Like Syndrome Due to Point Mutation

Publications for Prader-Willi-Like Syndrome Due to Point Mutation

Variations for Prader-Willi-Like Syndrome Due to Point Mutation

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

Search GEO for disease gene expression data for Prader-Willi-Like Syndrome Due to Point Mutation.

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

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

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

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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