Human Disease Ontology
19612 terms(s) returned
| Term Type: Class | Record: 1 to 50 of 19612 Records | Page: 1 of 393, First Previous Next Last | Show Records Per Page |
- (-)-carvone
- 1,2,4-triazines
- 1,2,5,6,9,10-hexabromocyclododecane
- 1,3-thiazoles
- 1,4-phenylenediamine
- 1,4-phenylenediamine allergic contact dermatitis
- 1-chloro-2,4-dinitrobenzene
- 1-chloro-2,4-dinitrobenzene allergic contact dermatitis
- 17-beta hydroxysteroid dehydrogenase 3 deficiency
- 2,4-dinitrophenyl allergic contact dermatitis
- 2,4-dinitrophenyl group
- 2,6-diaminopurines
- 2-aminoadipic 2-oxoadipic aciduria
- 2-benzofurans
- 2-hydroxyglutaric aciduria
- 2KB_downstream_variant
- 2KB_upstream_variant
- 3,3',5,5'-tetrabromobisphenol A
- 3-(carbamoyloxymethyl)cephalosporin
- 3-M syndrome
- 3-hydroxy steroid
- 3-hydroxy-3-methylglutaryl-CoA lyase deficiency
- 3-hydroxyisobutryl-CoA hydrolase deficiency
- 3-methylcrotonyl-CoA carboxylase 1 deficiency
- 3-methylcrotonyl-CoA carboxylase 2 deficiency
- 3-methylcrotonyl-CoA carboxylase deficiency
- 3-methylglutaconic aciduria
- 3-methylglutaconic aciduria type 1
- 3-methylglutaconic aciduria type 3
- 3-methylglutaconic aciduria type 4
- 3-methylglutaconic aciduria type 5
- 3-methylglutaconic aciduria type 7a
- 3-methylglutaconic aciduria type 7b
- 3-methylglutaconic aciduria type 8
- 3-methylglutaconic aciduria type 9
- 3-methylglutaconic aciduria with cataracts, neurologic involvement and neutropenia
- 3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome
- 3D_polypeptide_structure_variant
- 3MC syndrome
- 3MC syndrome 1
- 3MC syndrome 2
- 3MC syndrome 3
- 3_prime_UTR_elongation
- 3_prime_UTR_exon_variant
- 3_prime_UTR_intron_variant
- 3_prime_UTR_truncation
- 3_prime_UTR_variant
- 3alpha-hydroxy steroid
- 3p deletion syndrome
- 4-tert-butylphenol
