Mondo Disease Ontology
5568 terms(s) returned
| Term Type: | Record: 4451 to 4500 of 5568 Records | Page: 90 of 112, First Previous Next Last | Show Records Per Page |
- congenital cataract-ichthyosis syndrome
- congenital cataract-microcephaly-nevus flammeus simplex-severe intellectual disability syndrome
- congenital cataract-progressive muscular hypotonia-hearing loss-developmental delay syndrome
- congenital cataract-severe neonatal hepatopathy-global developmental delay syndrome
- congenital cataracts-facial dysmorphism-neuropathy syndrome
- congenital cerebellar anomaly, non-human animal
- congenital cerebellar anomaly, pig
- congenital cerebellar ataxia due to RNU12 mutation
- congenital chylothorax
- congenital communicating hydrocephalus
- congenital complete agenesis of pericardium
- 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 deformities of limbs
- congenital diaphragmatic hernia
- 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 IIq
- congenital disorder of glycosylation, type IIr
- congenital disorder of glycosylation, type IIw
