C4551995 |
Mitochondrial DNA Depletion Syndrome 1
|
disease |
|
Disease or Syndrome
|
genetic disease; disease of metabolism
|
|
4 |
78 |
C1858424 |
Cardioencephalomyopathy, Fatal Infantile, due to Cytochrome C Oxidase Deficiency
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases; Nervous System Diseases; Cardiovascular Diseases
|
Disease or Syndrome
|
genetic disease; disease of metabolism
|
|
2 |
7 |
C0007193 |
Cardiomyopathy, Dilated
|
group |
Cardiovascular Diseases
|
Disease or Syndrome
|
genetic disease; disease of anatomical entity
|
Abnormality of the cardiovascular system
|
43 |
443 |
C0036572 |
Seizures
|
phenotype |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
|
Sign or Symptom
|
disease of anatomical entity
|
Abnormality of the nervous system
|
237 |
417 |
C1837148 |
MYOPIA 6 (disorder)
|
disease |
Eye Diseases
|
Disease or Syndrome
|
disease of anatomical entity
|
|
2 |
2 |
C1837397 |
Severe global developmental delay
|
phenotype |
|
Finding
|
|
Abnormality of the nervous system
|
33 |
50 |