Cell Line Ontology - Human Pluripotent Stem Cell Registry
179 terms(s) returned
Term Type: Class | Record: 51 to 100 of 179 Records | Page: 2 of 4, First Previous Next Last | Show Records Per Page |
- brain disease
- cancer
- carbohydrate metabolism disease
- carcinoma
- cardiomyopathy
- cardiovascular system disease
- catecholaminergic polymorphic ventricular tachycardia
- cell type cancer
- central nervous system disease
- cerebral degeneration
- chromosomal deletion syndrome
- chromosomal disease
- ciliopathy
- cognitive disorder
- communication disorder
- congenital hypoplastic anemia
- congenital muscular dystrophy
- congenital muscular dystrophy due to LMNA mutation
- connective tissue disease
- cystic fibrosis
- cystic kidney disease
- degeneration of macula and posterior pole
- dementia
- demyelinating disease
- dermatitis
- developmental disorder of mental health
- diabetes mellitus
- disease
- disease of anatomical entity
- disease of cellular proliferation
- disease of mental health
- disease of metabolism
- early infantile epileptic encephalopathy
- electroclinical syndrome
- endogenous depression
- epidermolysis bullosa
- epidermolysis bullosa simplex
- epilepsy
- erythromelalgia
- eye and adnexa disease
- eye disease
- focal segmental glomerulosclerosis
- fragile X syndrome
- frontotemporal dementia
- gangliosidosis
- genetic disease
- glomerulonephritis
- glomerulosclerosis
- glucose metabolism disease
- heart conduction disease