MUSCULAR DYSTROPHY, CARDIAC TYPE

General Information (adopted from Orphanet):

Synonyms, Signs:
Number of Symptoms 10
OrphanetNr:
OMIM Id: 309930
ICD-10:
UMLs:
MeSH:
MedDRA:
Snomed:

Prevalence, inheritance and age of onset:

Prevalence: No data available.
Inheritance: X-linked inheritance
[Omim]
Age of onset:

Disease classification (adopted from Orphanet):

Parent Diseases: No data available.

Symptom Information: Sort by abundance 

1
(HPO:0003167) Carnosinuria 3 / 7739
2
(HPO:0001638) Cardiomyopathy 192 / 7739
3
(HPO:0003115) Abnormal EKG 44 / 7739
4
(HPO:0003236) Elevated serum creatine phosphokinase 214 / 7739
5
(HPO:0003560) Muscular dystrophy 88 / 7739
6
(OMIM) Abnormal electrocardiograph 1 / 7739
7
(HPO:0001417) X-linked inheritance 173 / 7739
8
(OMIM) Normal neurologic status 1 / 7739
9
(OMIM) Apical systolic murmur 1 / 7739
10
(OMIM) Globular hypokinetic heart 1 / 7739

Associated genes:

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information: