|
gliosis, familial progressive subcortical
|
9096 |
|
|
autosomal recessive persistent hyperplastic primary vitreous
|
9097 |
|
|
obsolete rare pulmonary hypertension
|
19096.0 |
|
|
generalized familial semibenign, autosomal dominant BCG infection
|
C565909 |
|
|
ERCC6 UV-sensitive syndrome
|
10909 |
|
|
familial progressive subcortical gliosis
|
9096 |
|
|
inborn glutathione synthase activity disorder
|
17909 |
|
|
autosomal recessive syndrome of skin ulceration, arthroosteolysis with pseudoacromegaly, keratitis, and oligodontia
|
9095 |
|
|
inherited glutathione synthetase deficiency
|
17909 |
|
|
neonatal Bartter syndrome type 4B with sensorineural deafness
|
909 |
|
|
immunodeficiency due to selective anti-polysaccharide antibody deficiency
|
19093 |
|
|
antenatal Epstein-Barr virus infection
|
19094 |
|
