Mondo Disease Ontology
2122 terms(s) returned
| Term Type: | Record: 1 to 50 of 2122 Records | Page: 1 of 43, First Previous Next Last | Show Records Per Page |
- MAK-related retinopathy
- MALT lymphoma
- MAN1B1-congenital disorder of glycosylation
- MAN2B2 deficiency
- MASA syndrome
- MASS syndrome
- MCD diffuse large B-cell lymphoma
- MECOM-associated syndrome
- MED12-related intellectual disability syndrome
- MEDNIK syndrome
- MEGF10-related myopathy
- MEGF8-related Carpenter syndrome
- MEHMO syndrome
- MELAS syndrome
- MELAS syndrome caused by mutation in MTND1
- MELAS syndrome caused by mutation in MTND5
- MELAS syndrome caused by mutation in MTND6
- MELAS syndrome caused by mutation in MTTC
- MELAS syndrome caused by mutation in MTTH
- MELAS syndrome caused by mutation in MTTK
- MELAS syndrome caused by mutation in MTTL1
- MELAS syndrome caused by mutation in MTTQ
- MELAS syndrome caused by mutation in MTTS1
- MELAS syndrome caused by mutation in MTTS2
- MEND syndrome
- MERRF syndrome
- MERTK-related retinopathy
- MGAT2-congenital disorder of glycosylation
- MGP-related spondyloepiphyseal dysplasia
- MHC class I deficiency
- MHC class I deficiency 1
- MHC class I deficiency 2
- MHC class I deficiency 3
- MHC class II deficiency
- MHC class II deficiency 1
- MHC class II deficiency 2
- MHC class II deficiency 3
- MHC class II deficiency 4
- MHC class II deficiency 5
- MIR140-related spondyloepiphyseal dysplasia
- MIRAGE syndrome
- MIT family translocation renal cell carcinoma
- MKKS-related ciliopathy
- MME-related autosomal dominant Charcot Marie Tooth disease type 2
- MMEP syndrome
- MOGS-congenital disorder of glycosylation
- MOMO syndrome
- MONDO_0002393
- MONDO_0003683
- MONDO_0005248
