Cell Line Ontology
74 terms(s) returned
| Term Type: | Record: 1 to 50 of 74 Records | Page: 1 of 2, First Previous Next Last | Show Records Per Page |
- HYDROCEPHALUS, AGYRIA, AND RETINAL DYSPLASIA
- HYPOCHONDROPLASIA
- Hallervorden-Spatz syndrome
- Hartnup disease
- Hereditary choroidal atrophy
- Hereditary peripheral neuropathy
- Hereditary retinal dystrophy
- Hirschsprung's disease
- Hodgkin's lymphoma
- hair disease
- hamartoma
- hearing disorder
- 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
