|
congenital disorder of glycosylation, type III
|
13325 |
|
|
congenital disorder of glycosylation, type III; CDG2I
|
http://purl.obolibrary.org/obo/MONDO_0013325 |
|
|
malignant neoplasm of lung hilum
|
4332 |
|
|
malignant tumor of lung hilum
|
4332 |
|
|
malignant neoplasm of lung hilus
|
4332 |
|
|
ganglioneuroblastoma (disease) of peripheral nervous system
|
3327 |
|
|
familial, with propensity to acute myelogenous leukemia thrombocytopenia
|
C563324 |
|
|
hydrocephalus cleft palate joint contractures
|
C535332 |
|
|
muscle syndrome, piriformis
|
43320 |
|
|
muscle syndromes, piriformis
|
43320 |
|
|
deficiency of platelet fibrinogen receptor
|
31332 |
|
|
spleen disease or disorder
|
2332 |
|
|
type I punctate palmoplantar keratoderma
|
19332 |
|
|
obsolete stromal predominant kidney Wilms' tumor
|
3324.0 |
|
