Mondo Disease Ontology
3157 terms(s) returned
| Term Type: | Record: 1 to 50 of 3157 Records | Page: 1 of 64, First Previous Next Last | Show Records Per Page |
- C syndrome
- C-cell hyperplasia
- C1 inhibitor deficiency
- C1Q deficiency
- C1Q deficiency 1
- C1Q deficiency 2
- C1Q deficiency 3
- C1q nephropathy
- C3 glomerulonephritis
- CACNA1A-related complex neurodevelopmental disorder
- CACNA1F-related retinopathy
- CACNA2D4-related retinopathy
- CADDS
- CADINS disease
- CAMK2D-related neurodevelopmental disorder and dilated cardiomyopathy
- CAMOS syndrome
- CANOMAD syndrome
- CAPN5-related vitreoretinopathy
- CARASIL syndrome
- CBL-related disorder
- CCDC115-CDG
- CCNK-related neurodevelopmental disorder-severe intellectual disability-facial dysmorphism syndrome
- CD4+/CD56+ hematodermic neoplasm
- CDH1-related diffuse gastric and lobular breast cancer syndrome
- CDK4 linked melanoma
- CDKL5 disorder
- CEBALID syndrome
- CEBPE-associated autoinflammation-immunodeficiency-neutrophil dysfunction syndrome
- CEDNIK syndrome
- CELSR1-related late-onset primary lymphedema
- CEP290-related ciliopathy
- CERKL-related retinopathy
- CGF1
- CHAND syndrome
- CHARGE syndrome
- CHEK2-related cancer predisposition
- CHILD syndrome
- CHIME syndrome
- CHRNG-associated hypo-akinesia disorder of prenatal onset
- CIC-rearranged sarcoma
- CIDEC-related familial partial lipodystrophy
- CINCA syndrome
- CK syndrome
- CLAPO syndrome
- CLOVES syndrome
- CNGA1-related retinopathy
- CNGA3-related retinopathy
- CNGB1-related retinopathy
- CNGB3-related retinopathy
- CNS demyelinating autoimmune disease
