Experimental Factor Ontology
1414 terms(s) returned
| Term Type: | Record: 1 to 50 of 1414 Records | Page: 1 of 29, First Previous Next Last | Show Records Per Page |
- C syndrome
- C1 inhibitor deficiency
- C1Q deficiency
- C1Q deficiency 1
- C3 glomerulonephritis
- CACNA1A-related complex neurodevelopmental disorder
- CACNA1F-related retinopathy
- CADDS
- CAMOS syndrome
- CARASIL syndrome
- CBL-related disorder
- CCDC115-CDG
- CDH1-related diffuse gastric and lobular breast cancer syndrome
- CDKL5 disorder
- CEBALID syndrome
- CEDNIK syndrome
- CEP290-related ciliopathy
- CHAND syndrome
- CHARGE syndrome
- CHEK2-related cancer predisposition
- CHILD syndrome
- CHIME syndrome
- CIC-rearranged sarcoma
- CIDEC-related familial partial lipodystrophy
- CINCA syndrome
- CK syndrome
- CLAPO syndrome
- CLOVES syndrome
- CODAS syndrome
- COFS syndrome
- COG1-congenital disorder of glycosylation
- COG4-congenital disorder of glycosylation
- COG5-congenital disorder of glycosylation
- COG6-congenital disorder of glycosylation
- COG7-congenital disorder of glycosylation
- COG8-congenital disorder of glycosylation
- COL4A1-related disorder
- COVID-19
- CPOX-related hereditary coproporphyria
- CTNNB1-related neurodevelopmental disorder and/or vitreoretinopathy
- CTSC-related disorder
- Caffey disease
- Camptosynpolydactyly, complex
- Camurati-Engelmann disease
- Canavan disease
- Carey-Fineman-Ziter syndrome
- Carney complex
- Carney complex - trismus - pseudocamptodactyly syndrome
- Carney complex, type 1
- Carney triad
