|
pseudohypoaldosteronism type 2 caused by mutation in Cul3
|
13782 |
|
|
pseudohypoaldosteronism type 2 caused by mutation in KLHL3
|
13781 |
|
|
shields type 2 dentin dyspalsia
|
D003784 |
|
|
teratoma, benign (morphologic abnormality)
|
2378 |
|
|
congenital motor, 2 nystagmus
|
C537854 |
|
|
pseudohypoaldosteronism type 2D
|
13781 |
|
|
partial deletion (short arm) chromosome 8
|
C537826 |
|
|
deficiency of 3-beta-hydroxysteroid-delta(5)-desaturase
|
C537880 |
|
|
fibromatosis, gingival, 3; GINGF3
|
http://purl.obolibrary.org/obo/MONDO_0012378 |
|
|
orofacial cleft 10; OFC10
|
http://purl.obolibrary.org/obo/MONDO_0013378 |
|
|
retinitis pigmentosa 63; RP63
|
http://purl.obolibrary.org/obo/MONDO_0013780 |
|
