Experimental Factor Ontology
3115 terms(s) returned
| Term Type: | Record: 3051 to 3100 of 3115 Records | Page: 62 of 63, First Previous Next Last | Show Records Per Page |
- hypotensive disorder
- hypothalamic disorder
- hypothalamic hamartomas with gelastic seizures
- hypothalamic neoplasm
- hypothalamus
- hypothyroidism
- hypothyroidism due to TSH receptor mutations
- hypothyroidism due to deficient transcription factors involved in pituitary development or function
- hypothyroidism, congenital, nongoitrous
- hypothyroidism, congenital, nongoitrous, 2
- hypothyroidism, congenital, nongoitrous, 5
- hypothyroidism, congenital, nongoitrous, 7
- hypothyroidism, congenital, nongoitrous, 8
- hypothyroidism, congenital, nongoitrous, 9
- hypotonia with lactic acidemia and hyperammonemia
- hypotonia, ataxia, and delayed development syndrome
- hypotonia, ataxia, developmental delay, and tooth enamel defect syndrome
- hypotonia, hypoventilation, impaired intellectual development, dysautonomia, epilepsy, and eye abnormalities
- hypotonia, infantile, with psychomotor retardation and characteristic facies
- hypotonia, infantile, with psychomotor retardation and characteristic facies 1
- hypotonia, infantile, with psychomotor retardation and characteristic facies 3
- hypotonia-cystinuria syndrome
- hypotonia-failure to thrive-microcephaly syndrome
- hypotrichosis
- hypotrichosis 1
- hypotrichosis 14
- hypotrichosis 15
- hypotrichosis 2
- hypotrichosis 3
- hypotrichosis 4
- hypotrichosis 5
- hypotrichosis 6
- hypotrichosis 7
- hypotrichosis 8
- hypotrichosis of eyelid
- hypotrichosis simplex
- hypotrichosis simplex of the scalp
- hypotrichosis-deafness syndrome
- hypotrichosis-intellectual disability, Lopes type
- hypotrichosis-lymphedema-telangiectasia syndrome (grouping)
- hypotrichosis-osteolysis-periodontitis-palmoplantar keratoderma syndrome
- hypotropia
- hypouricemia, renal
- hypouricemia, renal, 2
- hypoxanthine
- hypoxanthine guanine phosphoribosyltransferase partial deficiency
- hypoxanthine measurement
- hypoxanthine-guanine phosphoribosyltransferase
- hypoxanthine-guanine phosphoribosyltransferase (human)
- hypoxanthine-guanine phosphoribosyltransferase deficiency
