Cell Line Ontology
927 terms(s) returned
| Term Type: | Record: 1 to 50 of 927 Records | Page: 1 of 19, First Previous Next Last | Show Records Per Page |
- 46 XX gonadal dysgenesis
- 46 XY gonadal dysgenesis
- ACYL-CoA DEHYDROGENASE, MEDIUM-CHAIN, deficiency OF
- ACYL-CoA DEHYDROGENASE, long-CHAIN, deficiency OF
- ADRENOLEUKODYSTROPHY, AUTOSOMAL NEONATAL FORM
- ALBINISM I
- AMAUROTIC FAMILY IDIOCY, JUVENILE type
- Alagille syndrome
- Albers-Schonberg disease
- Alexander disease
- Alpers syndrome
- Angelman syndrome
- Arteriovenous Malformations, Cerebral
- Askin's tumor
- B cell deficiency
- B-cell lymphoma
- Bardet-Biedl syndrome
- Beckwith-Wiedemann syndrome
- Bernard-Soulier syndrome
- Bloch Sulzberger syndrome
- Bruck-de Lange syndrome
- Burkitt lymphoma
- CD40 deficiency
- CNS demyelinating autoimmune disease
- COFS syndrome
- Canavan disease
- Carpus curvus
- Charcot-Marie-Tooth disease
- Chediak-Higashi syndrome
- Coffin-Lowry syndrome
- Congenital cerebellar hypoplasia
- Conjunctival degeneration
- Conjunctival degenerations and deposits
- Corneal dystrophy
- Cri-Du-Chat syndrome
- Crigler-Najjar syndrome
- Crouzon syndrome
- Cryptophthalmos
- DNA ligase IV deficiency
- DNA repair deficiency
- DNA virus infectious disease
- Denys-Drash syndrome
- DiGeorge syndrome
- Donohue Syndrome
- Dubowitz Syndrome
- EEC SYNDROME
- Ectopia Lentis
- Ehlers-Danlos syndrome
- Ellis-Van Creveld syndrome
- Endocardial Cushion Defects
