Mondo Disease Ontology
694 terms(s) returned
| Term Type: | Record: 1 to 50 of 694 Records | Page: 1 of 14, First Previous Next Last | Show Records Per Page |
- RAB18 deficiency
- RAB23-related Carpenter syndrome
- RAB28-related retinopathy
- RASopathy
- RCBTB1-related retinopathy
- RD3-related retinopathy
- RDH12-related dominant retinopathy
- RDH12-related recessive retinopathy
- RDH5-related retinopathy
- RECON progeroid syndrome
- RELA fusion-positive ependymoma
- REM sleep behavior disorder
- RET fusion positive cancer
- RFT1-congenital disorder of glycosylation
- RHYNS syndrome
- RIDDLE syndrome
- RIN2 syndrome
- RLBP1-related retinopathy
- RNASEH2A-related type 1 interferonopathy
- RNASEH2B-related type 1 interferonopathy
- RNASEH2C-related type 1 interferonopathy
- RNU7-1-related type 1 interferonopathy
- RP1-related dominant retinopathy
- RP1-related recessive retinopathy
- RP2-related retinopathy
- RPE65-related dominant retinopathy
- RPE65-related recessive retinopathy
- RPGR-related retinopathy
- RYR1-related myopathy
- Rabin-Pappas syndrome
- Rabson-Mendenhall syndrome
- Radio-Tartaglia syndrome
- Rafiq syndrome
- Rahman syndrome
- Rajab interstitial lung disease with brain calcifications
- Rajab interstitial lung disease with brain calcifications 1
- Rajab interstitial lung disease with brain calcifications 2
- Ramon syndrome
- Ramos-Arroyo syndrome
- Rapp-Hodgkin syndrome
- Rasmussen subacute encephalitis
- Rauch-Steindl syndrome
- Raynaud disease
- Reese retinal dysplasia
- Reis-Bucklers corneal dystrophy
- Renpenning syndrome
- Reoviridae infectious disease
- Reoviridae infectious disease, non-human animal
- Rett syndrome
- Rett syndrome, congenital variant
