Experimental Factor Ontology
1212 terms(s) returned
| Term Type: | Record: 1 to 50 of 1212 Records | Page: 1 of 25, First Previous Next Last | Show Records Per Page |
- A20 haploinsufficiency
- AA amyloidosis
- AApoAI amyloidosis
- ABCA4-related retinopathy
- ABCD syndrome
- ABeta amyloidosis, Arctic type
- ABeta amyloidosis, Iowa type
- ABeta amyloidosis, Italian type
- ABeta amyloidosis, dutch type
- ABeta2M amyloidosis
- ABetaA21G amyloidosis
- ABetaL34V amyloidosis
- ABri amyloidosis
- ACCES syndrome
- ACTB-associated syndromic thrombocytopenia
- ACTH-independent Cushing syndrome
- ACTH-independent adrenal Cushing syndrome, somatic
- ACTH-independent macronodular adrenal hyperplasia 1
- ACTH-producing pituitary gland neoplasm
- ACTL6A-related BAFopathy
- ACys amyloidosis
- ADAR-related type 1 interferonopathy
- ADNP-related multiple congenital anomalies - intellectual disability - autism spectrum disorder
- ADULT syndrome
- ADan amyloidosis
- AFib amyloidosis
- AGAT deficiency
- AICA-ribosiduria
- AKT2-related familial partial lipodystrophy
- AKT3-related overgrowth spectrum
- AL amyloidosis
- ALDH18A1-related de Barsy syndrome
- ALECT2 amyloidosis
- ALG1-congenital disorder of glycosylation
- ALG11-congenital disorder of glycosylation
- ALG12-congenital disorder of glycosylation
- ALG14-congenital disorder of glycosylation
- ALG2-congenital disorder of glycosylation
- ALG3-congenital disorder of glycosylation
- ALG6-congenital disorder of glycosylation 1C
- ALG8-congenital disorder of glycosylation
- ALG9-associated autosomal dominant polycystic kidney disease
- ALG9-congenital disorder of glycosylation
- ALS2-related motor neuron disease
- ALys amyloidosis
- AMED syndrome, digenic
- ANE syndrome
- AP-4 deficiency syndrome
- APC-related attenuated familial adenomatous polyposis
- AREDYLD syndrome
