|
hemolytic disease due to fetomaternal alloimmunization
|
17163 |
|
|
episodic ataxia, Nystagmus-associated
|
7163 |
|
|
autosomal dominant PROC deficiency
|
C567163 |
|
|
Nystagmus-associated episodic ataxia
|
7163 |
|
|
familial paroxysmal ataxia
|
7163 |
|
|
hereditary episodic ataxia caused by mutation in CACNA1A
|
7163 |
|
|
Acetazolamide-responsive episodic ataxia syndrome
|
7163 |
|
|
protein c deficiency, autosomal dominant
|
C567163 |
|
|
PANDAS pediatric autoimmune neuropsychiatric disorders associated with streptococcal infections
|
C537163 |
|
|
PROC deficiency, autosomal dominant
|
C567163 |
|
|
thrombophilia, hereditary, due to protein c deficiency, autosomal dominant
|
C567163 |
|
|
CACNA1A hereditary episodic ataxia
|
7163 |
|
