Experimental Factor Ontology
11977 terms(s) returned
Term Type: Class | Record: 101 to 150 of 11977 Records | Page: 3 of 240, First Previous Next Last | Show Records Per Page |
- 6q16 deletion syndrome
- 7p22.1 microduplication syndrome
- 7q11.23 microduplication syndrome
- 7q31 microdeletion syndrome
- 8p inverted duplication/deletion syndrome
- 8p11.2 deletion syndrome
- 8p23.1 duplication syndrome
- 8p23.1 microdeletion syndrome
- 8q12 microduplication syndrome
- 8q22.1 microdeletion syndrome
- 8q24.3 microdeletion syndrome
- 9p13 microdeletion syndrome
- 9q31.1q31.3 microdeletion syndrome
- 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
- 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