|
partial deletion of chromosome 9q
|
16908 |
|
|
partial monosomy of chromosome 9q
|
16908 |
|
|
meningioma (disease) of clivus of occipital bone
|
3908 |
|
|
congenital disorder of glycosylation type 2a
|
8908 |
|
|
congenital disorder of glycosylation type IIa
|
8908 |
|
|
congenital disorder of glycosylation, type IIa
|
8908 |
|
|
congenital disorder of glycosylation, type IIa; CDG2A
|
http://purl.obolibrary.org/obo/MONDO_0008908 |
|
|
partial monosomy of the long arm of chromosome 9
|
16908 |
|
|
thyrotoxic periodic paralysis, susceptibility to, 3
|
13908 |
|
|
thyrotoxic periodic paralysis, susceptibility to, 3; TTPP3
|
http://purl.obolibrary.org/obo/MONDO_0013908 |
|
|
smith lemli opitz syndrome
|
D019082 |
|
|
smith lemli opitz syndrome, type 1
|
D019082 |
|
|
smith lemli opitz syndrome, type 2
|
D019082 |
|
|
smith lemli opitz syndrome, type II
|
D019082 |
|
