Cell Line Ontology
927 terms(s) returned
Term Type: Class | Record: 451 to 500 of 927 Records | Page: 10 of 19, First Previous Next Last | Show Records Per Page |
- heart disease
- heart valve disease
- hemangioblastoma
- hemangioma
- hemangioma of skin
- hemangiopericytic tumor
- hematologic cancer
- hematological disorder of fetus and newborn
- hematopoietic system disease
- hemochromatosis
- hemoglobinopathy
- hemolytic anemia
- hemophagocytic lymphohistiocytosis
- hemophagocytic syndrome
- hemophilia
- hemophilia B
- hemorrhagic disorder
- hepatic porphyria
- hepatobiliary disease
- hepatobiliary system cancer
- hepatocellular carcinoma
- hepatoerythropoietic porphyria
- hepatolenticular degeneration
- hereditary and idiopathic peripheral neuropathy
- hereditary central nervous system demyelinating disease
- hereditary coproporphyria
- hereditary degenerative disease of central nervous system
- hereditary disease
- hereditary eye disease
- hereditary hemorrhagic telangiectasia
- hereditary hyperbilirubinemia
- hereditary motor and sensory neuropathy
- hereditary motor neuropathy proximal type I
- hereditary multiple exostoses
- hereditary neoplastic syndrome
- hereditary optic atrophy
- hereditary sensory and autonomic neuropathy
- hereditary spherocytosis
- hereditary urogenital adysplasia
- histiocytic and dendritic cell cancer
- histiocytosis
- holocarboxylase synthetase deficiency
- holoprosencephaly
- homocystinuria
- hyperargininemia
- hyperbilirubinemia
- hypercholesterolemia
- hyperlipidemia
- hyperlipoproteinemia
- hyperlipoproteinemia type III