|
congenital disorder of glycosylation, type i/IIx
|
8909 |
|
|
partial monosomy of the long arm of chromosome 10
|
16909 |
|
|
partial monosomy of the long arm of chromosome type 10
|
16909 |
|
|
obsolete rare pulmonary hypertension
|
19096.0 |
|
|
Pestivirus disease or disorder
|
5909 |
|
|
type a4 postaxial polydactyly
|
C563909 |
|
|
persistent hyperplastic primary vitreous, autosomal recessive
|
9097 |
|
|
persistent hyperplastic primary vitreous, autosomal recessive; PHPVAR
|
http://purl.obolibrary.org/obo/MONDO_0009097 |
|
|
ciliary dyskinesia, primary, 34
|
14909 |
|
|
ciliary dyskinesia, primary, 34, without situs inversus
|
14909 |
|
|
ciliary dyskinesia, primary, 34; CILD34
|
http://purl.obolibrary.org/obo/MONDO_0014909 |
|
|
autosomal recessive persistent hyperplastic primary vitreous
|
9097 |
|
|
non-acquired combined pituitary hormone deficiency with spine abnormalities
|
9091 |
|
|
non-acquired combined pituitary hormone deficiency-deafness-rigid cervical spine syndrome
|
9091 |
|
|
non-acquired combined pituitary hormone deficiency-sensorineural hearing loss-spine abnormalities syndrome
|
9091 |
|
