Experimental Factor Ontology
687 terms(s) returned
Term Type: Class | Record: 651 to 687 of 687 Records | Page: 14 of 14, First Previous Next Last | Show Records Per Page |
- hypoplastic left heart syndrome
- hypoplastic left heart syndrome 1
- hypoplastic left heart syndrome 2
- hypoplastic pancreas-intestinal atresia-hypoplastic gallbalder syndrome
- hyposmia-nasal and ocular hypoplasia-hypogonadotropic hypogonadism syndrome
- hypospadias-intellectual disability, Goldblatt type syndrome
- hypothalamic disorder
- hypothalamic hamartomas with gelastic seizures
- hypothyroidism due to TSH receptor mutations
- hypothyroidism due to deficient transcription factors involved in pituitary development or function
- hypothyroidism, congenital, nongoitrous
- hypothyroidism, congenital, nongoitrous, 5
- hypothyroidism, congenital, nongoitrous, 7
- hypotonia with lactic acidemia and hyperammonemia
- 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-cystinuria syndrome
- hypotonia-failure to thrive-microcephaly syndrome
- hypotrichosis
- hypotrichosis 2
- hypotrichosis 3
- hypotrichosis 4
- hypotrichosis 5
- 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 guanine phosphoribosyltransferase partial deficiency
- hypoxanthine-guanine phosphoribosyltransferase deficiency