Human Disease Ontology
1950 terms(s) returned
| Term Type: | Record: 1501 to 1550 of 1950 Records | Page: 31 of 39, First Previous Next Last | Show Records Per Page |
- congenital disorder of glycosylation type IIp
- congenital disorder of glycosylation type IIq
- congenital disorder of glycosylation type IIr
- congenital disorder of glycosylation type IIt
- congenital disorder of glycosylation type IIv
- congenital disorder of glycosylation type IIw
- congenital disorder of glycosylation type IIy
- congenital disorder of glycosylation type IIz
- congenital dyserythropoietic anemia
- congenital dyserythropoietic anemia type I
- congenital dyserythropoietic anemia type II
- congenital dyserythropoietic anemia type IIIa
- congenital dyserythropoietic anemia type IIIb
- congenital dyserythropoietic anemia type IVa
- congenital dyserythropoietic anemia type IVb
- congenital dyserythropoietic anemia type Ia
- congenital dyserythropoietic anemia type Ib
- congenital epulis
- congenital fibrosarcoma
- congenital fibrosis of the extraocular muscles
- congenital fibrosis of the extraocular muscles 1
- congenital fibrosis of the extraocular muscles 2
- congenital fibrosis of the extraocular muscles 3A
- congenital fibrosis of the extraocular muscles 3C
- congenital fibrosis of the extraocular muscles 5
- congenital generalized lipodystrophy
- congenital generalized lipodystrophy type 1
- congenital generalized lipodystrophy type 2
- congenital generalized lipodystrophy type 3
- congenital generalized lipodystrophy type 4
- congenital glutamine deficiency
- congenital granular cell tumor
- congenital heart block
- congenital heart defects, dysmorphic facial features, and intellectual developmental disorder
- congenital heart defects, hamartomas of tongue, and polysyndactyly
- congenital heart disease
- congenital hemolytic anemia
- congenital hereditary endothelial dystrophy of cornea
- congenital hypogammaglobulinemia
- congenital hypoplastic anemia
- congenital hypothyroidism
- congenital hypotrichosis with juvenile macular dystrophy
- congenital intrinsic factor deficiency
- congenital kyphosis
- congenital lactase deficiency
- congenital leptin deficiency
- congenital limbs-face contractures-hypotonia-developmental delay syndrome
- congenital malabsorptive diarrhea 4
- congenital megabladder
- congenital merosin-deficient muscular dystrophy 1A
