Experimental Factor Ontology
54935 terms(s) returned
| Term Type: Class | Record: 27601 to 27650 of 54935 Records | Page: 553 of 1099, First Previous Next Last | Show Records Per Page |
- hypertelorism, microtia, facial clefting syndrome
- hypertelorism-preauricular sinus-punctual pits-deafness syndrome
- hypertension
- hypertension, pregnancy-induced
- hypertensive disorder
- hypertensive encephalopathy
- hypertensive heart disease
- hypertensive nephropathy
- hypertensive retinopathy
- hyperthyroidism
- hyperthyroxinemia
- hypertrichosis
- hypertrichosis cubiti-short stature syndrome
- hypertrichosis lanuginosa congenita
- hypertrichosis of eyelid
- hypertrichosis-acromegaloid facial appearance syndrome
- hypertrichotic osteochondrodysplasia Cantu type
- hypertriglyceridemia 2
- hypertrophic cardiomyopathy
- hypertrophic cardiomyopathy 1
- hypertrophic cardiomyopathy 10
- hypertrophic cardiomyopathy 11
- hypertrophic cardiomyopathy 12
- hypertrophic cardiomyopathy 13
- hypertrophic cardiomyopathy 14
- hypertrophic cardiomyopathy 15
- hypertrophic cardiomyopathy 17
- hypertrophic cardiomyopathy 19
- hypertrophic cardiomyopathy 2
- hypertrophic cardiomyopathy 20
- hypertrophic cardiomyopathy 25
- hypertrophic cardiomyopathy 26
- hypertrophic cardiomyopathy 4
- hypertrophic cardiomyopathy 6
- hypertrophic cardiomyopathy 7
- hypertrophic cardiomyopathy 9
- hypertrophic cardiomyopathy and renal tubular disease due to mitochondrial DNA mutation
- hypertrophic osteoarthropathy, primary, autosomal recessive, 1
- hypertrophy
- hyperuricemia
- hyperuricemia-pulmonary hypertension-renal failure-alkalosis syndrome
- hyperuricemic nephropathy, familial juvenile type 3
- hyperuricemic nephropathy, familial juvenile type 4
- hypervalinemia and hyperleucine-isoleucinemia
- hypervitaminosis A
- hyphal cell
- hypnic headache
- hypo- and hypermelanotic cutaneous macules-retarded growth-intellectual disability syndrome
- hypoaldosteronism disease
- hypoalphalipoproteinemia
