C0007193 |
Cardiomyopathy, Dilated
|
group |
Cardiovascular Diseases
|
Disease or Syndrome
|
genetic disease; disease of anatomical entity
|
Abnormality of the cardiovascular system
|
43 |
443 |
C1858763 |
Cardiomyopathy, Dilated, 1g
|
disease |
Cardiovascular Diseases
|
Disease or Syndrome
|
genetic disease; disease of anatomical entity
|
|
2 |
306 |
C1837342 |
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2J
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases
|
Disease or Syndrome
|
disease of anatomical entity
|
|
2 |
230 |
C1838244 |
TIBIAL MUSCULAR DYSTROPHY, TARDIVE
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases
|
Disease or Syndrome
|
genetic disease; disease of anatomical entity
|
|
2 |
17 |
C1863599 |
Hereditary Myopathy with Early Respiratory Failure
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Respiratory Tract Diseases; Nervous System Diseases
|
Disease or Syndrome
|
disease of anatomical entity
|
|
2 |
15 |
C2673677 |
Myopathy, Early-Onset, with Fatal Cardiomyopathy
|
disease |
Musculoskeletal Diseases; Nervous System Diseases; Cardiovascular Diseases
|
Disease or Syndrome
|
|
|
2 |
11 |
C1861065 |
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 9
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
Disease or Syndrome
|
disease of anatomical entity
|
|
2 |
7 |