Mondo Disease Ontology
5519 terms(s) returned
| Term Type: | Record: 4151 to 4200 of 5519 Records | Page: 84 of 111, First Previous Next Last | Show Records Per Page |
- complement component 3 deficiency, domestic guinea pig
- complement component 3 deficiency, non-human animal
- complement component 3 deficiency, rabbit
- complement component 4 deficiency, domestic guinea pig
- complement component 4 deficiency, non-human animal
- complement component 4a deficiency
- complement component 4b deficiency
- complement component 5 deficiency
- complement component 6 deficiency
- complement component 6 deficiency, non-human animal
- complement component 6 deficiency, rabbit
- complement component 7 deficiency
- complement component 9 deficiency
- complement component C1r/C1s deficiency
- complement component C1s deficiency
- complement deficiency
- complement factor H deficiency
- complement factor I deficiency
- complement factor b deficiency
- complement receptor activity
- complement receptor deficiency
- complement receptor mediated signaling pathway
- complete
- complete androgen insensitivity syndrome
- complete atrioventricular canal
- complete atrioventricular canal-left heart obstruction syndrome
- complete atrioventricular canal-tetralogy of fallot syndrome
- complete atrioventricular canal-ventricle hypoplasia syndrome
- complete cryptophthalmia
- complete hemimelia
- complete hydatidiform mole
- complete septate uterus
- complete trisomy 13
- complete trisomy 18
- complete trisomy 21
- complex cortical dysplasia with other brain malformations
- complex cortical dysplasia with other brain malformations 1
- complex cortical dysplasia with other brain malformations 2
- complex cortical dysplasia with other brain malformations 3
- complex cortical dysplasia with other brain malformations 4
- complex cortical dysplasia with other brain malformations 5
- complex cortical dysplasia with other brain malformations 6
- complex cortical dysplasia with other brain malformations 7
- complex endometrial hyperplasia
- complex hereditary spastic paraplegia
- complex lethal osteochondrodysplasia
- complex neurodevelopmental disorder
- complex neurodevelopmental disorder with motor features
- complex neurodevelopmental disorder with or without congenital anomalies
- complex of collagen trimers
