|
congenital erythropoietic porphyria
|
9902 |
|
|
optic neuritides, posterior
|
D009902 |
|
|
optic neuritis, posterior
|
D009902 |
|
|
rhizomelic chondrodysplasia punctatas
|
D018902 |
|
|
aortic valve, quadricuspid
|
D000082902 |
|
|
nut allergic reaction of pigmented ciliary epithelial cell
|
5902 |
|
|
IFNGR2 autosomal recessive mendelian susceptibility to mycobacterial diseases due to a partial deficiency
|
17902 |
|
|
cortical blindness, retardation, and postaxial polydactyly
|
9024 |
|
|
chondrodysplasia punctata, rhizomelic
|
D018902 |
|
|
chondrodysplasia punctatas, rhizomelic
|
D018902 |
|
|
nasopharyngeal carcinoma, susceptibility to, 3
|
14902.0 |
|
|
nasopharyngeal carcinoma, susceptibility to, 3; NPCA3
|
http://purl.obolibrary.org/obo/MONDO_0014902 |
|
|
nasopharyngeal carcinoma, susceptibility to, type 3
|
http://purl.obolibrary.org/obo/MONDO_0014902 |
|
