C0752124 |
Spinocerebellar Ataxia Type 6 (disorder)
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
|
Disease or Syndrome
|
genetic disease; disease of anatomical entity
|
|
64 |
11 |
C3887485 |
MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 1
|
phenotype |
|
Finding
|
disease of anatomical entity
|
|
20 |
19 |
C1720416 |
Episodic ataxia type 2 (disorder)
|
disease |
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases
|
Disease or Syndrome
|
disease of anatomical entity
|
|
13 |
60 |
C1832884 |
Hemiplegic migraine, familial type 1
|
disease |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
|
Disease or Syndrome
|
disease of anatomical entity
|
|
10 |
37 |
C4310716 |
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 42
|
disease |
|
Disease or Syndrome
|
disease of anatomical entity
|
|
1 |
28 |