Mondo Disease Ontology
6020 terms(s) returned
| Term Type: | Record: 4801 to 4850 of 6020 Records | Page: 97 of 121, First Previous Next Last | Show Records Per Page |
- congenital contractural arachnodactyly
- congenital contractures
- congenital contractures of the limbs and face, hypotonia, and developmental delay
- congenital copper deficiency, goat
- congenital copper deficiency, non-human animal
- congenital corneal opacities, cornea guttata, and corectopia
- congenital coronary artery aneurysm
- congenital craniosynostosis maternal hyperthyroiditis
- congenital cystic eye
- congenital cystic eye multiple ocular and intracranial anomalies
- congenital cystic eye, horse
- congenital deformities of limbs
- congenital diaphragmatic hernia
- congenital diaphragmatic hernia, non-human animal
- congenital diarrhea
- congenital diarrhea 5 with tufting enteropathy
- congenital diarrhea 6
- congenital diarrhea 7 with exudative enteropathy
- congenital disorder of deglycosylation
- congenital disorder of deglycosylation 1
- congenital disorder of deglycosylation 2
- congenital disorder of glycosylation
- congenital disorder of glycosylation syndrome type 4
- congenital disorder of glycosylation type 1E
- congenital disorder of glycosylation type 1EE with or without immunodeficiency
- congenital disorder of glycosylation type I
- congenital disorder of glycosylation type II
- congenital disorder of glycosylation with defective fucosylation
- congenital disorder of glycosylation with defective fucosylation 1
- congenital disorder of glycosylation with defective fucosylation 2
- congenital disorder of glycosylation, GALNT2-related, cattle
- congenital disorder of glycosylation, non-human animal
- congenital disorder of glycosylation, type 1DD
- congenital disorder of glycosylation, type 2v
- congenital disorder of glycosylation, type IAA
- congenital disorder of glycosylation, type ICC
- congenital disorder of glycosylation, type IIaa
- congenital disorder of glycosylation, type IIbb
- congenital disorder of glycosylation, type IIcc
- congenital disorder of glycosylation, type IIq
- congenital disorder of glycosylation, type IIr
- congenital disorder of glycosylation, type IIw
- congenital disorder of glycosylation, type IIy
- congenital disorder of glycosylation, type IIz
- congenital disorder of glycosylation, type Ibb
- congenital disorder of glycosylation, type Iw, autosomal dominant
- congenital disorder of glycosylation, type i/IIx
- congenital disorder of glycosylation, type iit
- congenital dyserythropoietic anemia
- congenital dyserythropoietic anemia type 1
