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, Skin diseases

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

MalaCards integrated aliases for Prader-Willi Syndrome Due to Paternal 15q11q13 Deletion:

Name: Prader-Willi Syndrome Due to Paternal 15q11q13 Deletion 58

Classifications:

Orphanet: 58  
Rare neurological diseases
Rare infertility disorders
Rare gynaecological and obstetric diseases
Rare endocrine diseases
Developmental anomalies during embryogenesis


External Ids:

ICD10 via Orphanet 33 Q87.1
Orphanet 58 ORPHA98793

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

MalaCards based summary : Prader-Willi Syndrome Due to Paternal 15q11q13 Deletion Affiliated tissues include skin.

Related Diseases for Prader-Willi Syndrome Due to Paternal 15q11q13 Deletion

Symptoms & Phenotypes for Prader-Willi Syndrome Due to Paternal 15q11q13 Deletion

Drugs & Therapeutics for Prader-Willi Syndrome Due to Paternal 15q11q13 Deletion

Search Clinical Trials , NIH Clinical Center for Prader-Willi Syndrome Due to Paternal 15q11q13 Deletion

Genetic Tests for Prader-Willi Syndrome Due to Paternal 15q11q13 Deletion

Anatomical Context for Prader-Willi Syndrome Due to Paternal 15q11q13 Deletion

MalaCards organs/tissues related to Prader-Willi Syndrome Due to Paternal 15q11q13 Deletion:

40
Skin

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

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

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

Search GEO for disease gene expression data for Prader-Willi Syndrome Due to Paternal 15q11q13 Deletion.

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

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
19 FMA
28 GO
29 GTR
30 HMDB
31 HPO
32 ICD10
33 ICD10 via Orphanet
34 ICD9CM
35 IUPHAR
36 KEGG
37 LifeMap
39 LOVD
41 MedGen
43 MeSH
44 MESH via Orphanet
45 MGI
48 NCI
49 NCIt
50 NDF-RT
53 NINDS
54 Novoseek
56 OMIM
57 OMIM via Orphanet
61 PubMed
63 QIAGEN
68 SNOMED-CT via HPO
69 TGDB
70 Tocris
71 UMLS
72 UMLS via Orphanet
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