Experimental Factor Ontology
94656 terms(s) returned
| Term Type: | Record: 8701 to 8750 of 94656 Records | Page: 175 of 1894, First Previous Next Last | Show Records Per Page |
- Congenital anonychia
- Congenital aphakia
- Congenital atransferrinemia
- Congenital bile acid synthesis defect type 1
- Congenital bile acid synthesis defect type 2
- Congenital bile acid synthesis defect type 3
- Congenital bile acid synthesis defect type 4
- Congenital cataract - hypertrophic cardiomyopathy - mitochondrial myopathy
- Congenital cataract - ichthyosis
- Congenital cataract - progressive muscular hypotonia - hearing loss - developmental delay
- Congenital cataract microcornea with corneal opacity
- Congenital cataracts - facial dysmorphism - neuropathy
- Congenital chloride diarrhea
- Congenital chronic diarrhea with protein-losing enteropathy
- Congenital deficiency in alpha-fetoprotein
- Congenital disorder of glycosylation with cardiac malformation as a major feature
- Congenital disorder of glycosylation with deafness as a major feature
- Congenital disorder of glycosylation with developmental anomaly
- Congenital disorder of glycosylation with dilated cardiomyopathy
- Congenital disorder of glycosylation with epilepsy as a major feature
- Congenital disorder of glycosylation with hepatic involvement
- Congenital disorder of glycosylation with intestinal involvement
- Congenital disorder of glycosylation with nephropathy as a major feature
- Congenital disorder of glycosylation with neurological involvement
- Congenital disorder of glycosylation with skin involvement
- Congenital dyserythropoietic anemia type I
- Congenital dyserythropoietic anemia type II
- Congenital dyserythropoietic anemia type III
- Congenital dyserythropoietic anemia type IV
- Congenital erythropoietic porphyria
- Congenital factor II deficiency
- Congenital finger flexion contractures
- Congenital generalized hypertrichosis, Ambras type
- Congenital hemolytic anemia
- Congenital hereditary facial paralysis with variable hearing loss
- Congenital hip dislocation
- Congenital hypothyroidism due to developmental anomaly
- Congenital ichthyosis - intellectual disability - spastic quadriplegia
- Congenital ichthyosis - microcephalus - tetraplegia
- Congenital intestinal disease due to an enzymatic defect
- Congenital intestinal motility disorder
- Congenital intrauterine infection-like syndrome
- Congenital intrinsic factor deficiency
- Congenital isolated thyroxine-binding globulin deficiency
- Congenital joint dislocations
- Congenital lactic acidosis
- Congenital lethal myopathy, Compton-North type
- Congenital malabsorptive diarrhea due to paucity of enteroendocrine cells
- Congenital microcephaly-severe encephalopathy-progressive cerebral atrophy syndrome
- Congenital miosis
