Mondo Disease Ontology
3899 terms(s) returned
Term Type: Class | Record: 151 to 200 of 3899 Records | Page: 4 of 78, First Previous Next Last | Show Records Per Page |
- SIM1-related Prader-Willi-like syndrome
- SIN3A
- SIN3A-related intellectual disability syndrome
- SIN3A-related intellectual disability syndrome due to a point mutation
- SIPA1L3
- SIX1
- SIX3
- SIX5
- SIX6
- SKI
- SKIC2
- SKIC3
- SLC10A2
- SLC10A7
- SLC10A7-congenital disorder of glycosylation
- SLC11A1
- SLC11A2
- SLC12A1
- SLC12A2-related autosomal dominant infantile-developmental delay-intellectual disability-sensorineural deafness syndrome
- SLC12A2-related autosomal recessive neonatal-developmental delay-intellectual disability-feeding difficulty-sensorineural deafness syndrome
- SLC12A2-related developmental delay-intellectual disability-sensorineural deafness syndrome
- SLC12A3
- SLC12A5
- SLC12A6
- SLC13A5
- SLC16A1
- SLC16A12
- SLC16A2
- SLC17A5
- SLC17A8
- SLC17A9
- SLC18A3
- SLC19A2
- SLC19A3
- SLC1A1
- SLC1A2
- SLC1A3
- SLC1A4
- SLC20A2
- SLC22A12
- SLC22A18
- SLC22A4
- SLC22A5
- SLC24A1
- SLC24A4
- SLC25A1
- SLC25A12
- SLC25A13
- SLC25A15
- SLC25A19