|
hereditary, due to protein c deficiency, autosomal dominant thrombophilia
|
C567163 |
|
|
hemolytic disease of the fetus and newborn
|
17163 |
|
|
Cerebellopathy, hereditary paroxysmal
|
7163 |
|
|
ataxia, familial paroxysmal
|
7163 |
|
|
ataxia, familial, paroxysmal
|
7163 |
|
|
Acetazolamide-responsive hereditary paroxysmal cerebellar ataxia
|
7163 |
|
|
cerebellar ataxia, paroxysmal, Acetazolamide-responsive
|
7163 |
|
|
Acetazolamide-responsive, hereditary, paroxysmal, cerebellar ataxia
|
7163 |
|
|
autosomal dominant protein c deficiency
|
C567163 |
|
|
episodic ataxia, type 2; EA2
|
http://purl.obolibrary.org/obo/MONDO_0007163 |
|
|
ataxia, episodic, with Nystagmus
|
7163 |
|
|
episodic ataxia with nystagmus
|
7163 |
|
