Cell Line Ontology - Human Pluripotent Stem Cell Registry
179 terms(s) returned
| Term Type: Class | Record: 1 to 50 of 179 Records | Page: 1 of 4, First Previous Next Last | Show Records Per Page |
- Alport syndrome
- Alzheimer's disease
- Bardet-Biedl syndrome
- Brugada syndrome
- CADASIL
- Danon disease
- Down syndrome
- Dravet syndrome
- Duchenne muscular dystrophy
- Fanconi anemia
- GM2 gangliosidosis
- Gaucher's disease
- Huntington's disease
- Joubert syndrome
- Kabuki syndrome
- Machado-Joseph disease
- Marfan syndrome
- Parkinson's disease
- Pelizaeus-Merzbacher disease
- Rubinstein-Taybi syndrome
- Smith-Magenis syndrome
- Tay-Sachs disease
- Usher syndrome
- X-linked dominant disease
- X-linked monogenic disease
- X-linked recessive disease
- acquired metabolic disease
- adenocarcinoma
- age related macular degeneration
- agnosia
- amyotrophic lateral sclerosis
- anemia
- anxiety disorder
- aplastic anemia
- arrhythmogenic right ventricular cardiomyopathy
- atopic dermatitis
- autism spectrum disorder
- autistic disorder
- autoimmune disease of central nervous system
- autoimmune disease of the nervous system
- autoimmune hypersensitivity disease
- autosomal dominant cerebellar ataxia
- autosomal dominant disease
- autosomal dominant polycystic kidney disease
- autosomal genetic disease
- autosomal recessive disease
- autosomal recessive osteopetrosis 4
- bipolar disorder
- bone disease
- bone remodeling disease
