MCID: RRF013
MIFTS: 7

Rare Familial Disorder with Hypertrophic Cardiomyopathy

Categories: Cardiovascular diseases, Genetic diseases, Rare diseases

Aliases & Classifications for Rare Familial Disorder with Hypertrophic Cardiomyopathy

MalaCards integrated aliases for Rare Familial Disorder with Hypertrophic Cardiomyopathy:

Name: Rare Familial Disorder with Hypertrophic Cardiomyopathy 58
Rare Familial Disorder with Hypertrophic Obstructive Cardiomyopathy 58
Rare Familial Disorder with Hypertrophic Subaortic Stenosis 58

Characteristics:

Orphanet epidemiological data:

58

Classifications:



External Ids:

MESH via Orphanet 45 D024741
UMLS via Orphanet 71 C0949658
Orphanet 58 ORPHA99739

Summaries for Rare Familial Disorder with Hypertrophic Cardiomyopathy

MalaCards based summary : Rare Familial Disorder with Hypertrophic Cardiomyopathy, is also known as rare familial disorder with hypertrophic obstructive cardiomyopathy.

Symptoms & Phenotypes for Rare Familial Disorder with Hypertrophic Cardiomyopathy

Drugs & Therapeutics for Rare Familial Disorder with Hypertrophic Cardiomyopathy

Search Clinical Trials , NIH Clinical Center for Rare Familial Disorder with Hypertrophic Cardiomyopathy

Genetic Tests for Rare Familial Disorder with Hypertrophic Cardiomyopathy

Anatomical Context for Rare Familial Disorder with Hypertrophic Cardiomyopathy

Publications for Rare Familial Disorder with Hypertrophic Cardiomyopathy

Variations for Rare Familial Disorder with Hypertrophic Cardiomyopathy

Expression for Rare Familial Disorder with Hypertrophic Cardiomyopathy

Search GEO for disease gene expression data for Rare Familial Disorder with Hypertrophic Cardiomyopathy.

Pathways for Rare Familial Disorder with Hypertrophic Cardiomyopathy

GO Terms for Rare Familial Disorder with Hypertrophic Cardiomyopathy

Sources for Rare Familial Disorder with Hypertrophic Cardiomyopathy

3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
17 EFO
18 ExPASy
19 FMA
20 GARD
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
44 MeSH
45 MESH via Orphanet
46 MGI
49 NCI
50 NCIt
51 NDF-RT
53 NINDS
54 Novoseek
56 OMIM via Orphanet
57 OMIM® (Updated 20-May-2021)
61 PubMed
63 QIAGEN
68 SNOMED-CT via HPO
69 Tocris
70 UMLS
71 UMLS via Orphanet
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