|
21 alpha hydroxylase deficiency
|
C535979 |
|
|
congenital adrenal hyperplasia due to 21 hydroxylase deficiency
|
C535979 |
|
|
endove syndrome, limb-brain type
|
30979 |
|
|
impairment of oral perception
|
9791 |
|
|
ALPS (autoimmune lymphoproliferative syndrome)
|
17979 |
|
|
adult-onset vitelliform macular dystrophy
|
11979 |
|
|
inclusion body myopathy, sporadic
|
D018979 |
|
|
inclusion body myositides
|
D018979 |
|
|
inclusion body myositis, sporadic
|
D018979 |
|
|
myoclonus, intractable, neonatal
|
14979 |
|
|
myoclonus, intractable, neonatal; NEIMY
|
14979 |
|
|
gyrate atrophy of choroid and retina
|
9796 |
|
|
hyperornithinemia-gyrate atrophy of choroid and retina syndrome
|
9796 |
|
|
gyrate atrophy of choroid and retina; GACR
|
http://purl.obolibrary.org/obo/MONDO_0009796 |
|
|
Girate atrophy of the retina
|
9796 |
|
