Cell Line Ontology
927 terms(s) returned
| Term Type: Class | Record: 501 to 550 of 927 Records | Page: 11 of 19, First Previous Next Last | Show Records Per Page |
- hyperlysinemia
- hyperuricemia
- hypochromic anemia
- hypogonadism
- hypohidrotic ectodermal dysplasia
- hypolipoproteinemia
- hypophospatasia, childhood
- hypophosphatasia
- hypophosphatemic rickets X-linked dominant
- hypoplastic left heart syndrome
- hypoprothrombinemia
- hypothalamic disease
- ichthyosis
- immune system cancer
- immune system disease
- immunoproliferative disorder
- inborn amino acid transport disorder
- inborn errors carbohydrate metabolism
- inborn errors fructose metabolism
- inborn errors lipid metabolism
- inborn errors metal metabolism
- inborn errors of amino acid metabolism
- inborn errors of metabolism
- inborn errors purine-pyrimidine metabolism
- inborn errors pyruvate metabolism
- inborn errors renal tubular transport
- inborn errors steroid metabolism
- inborn metabolic brain disease
- inborn urea cycle disorder
- infantile refsum disease
- inherited blood coagulation disorder
- integumentary system cancer
- integumentary system disease
- interstitial lung disease
- interstitial nephritis
- intestinal cancer
- intestinal disease
- intracranial aneurysm
- intracranial arterial disease
- intracranial neoplasm
- intrahepatic cholestasis
- invasive ductal carcinoma
- iron metabolism disorder
- iron overload
- islet cell tumor
- isovalericacidemia
- jaw abnormality
- jaw disease
- juvenile myoclonic epilepsy
- keratosis
