Label | Id |
---|
malignant osteopetrosis | 19026 | |
Taybi syndrome | 19027 | |
oto-palatal-digital syndrome | 19027 | |
oto-palato-digital syndrome | 19027 | |
otopalatodigital syndrome | 19027 | |
AP window | 21902 | |
aortic-pulmonary window | 21902 | |
aorto-pulmonary window | 21902 | |
aortopulmonary window | 21902 | |
type 2 (Andre syndrome) | http://purl.obolibrary.org/obo/MONDO_0019027 | |
cutaneous mastocytosis (disease) | 19023 | |
congenital hypogammaglobulinemia (finding) | 1902 | |
Charcot-Marie-Tooth disease, demyelinating, type 1F | 11902 | |
Charcot Marie Tooth disease type 1F | 11902 | |
osteopetrosis (disease), autosomal recessive | 19026 |