Mondo Disease Ontology
4118 terms(s) returned
| Term Type: | Record: 51 to 100 of 4118 Records | Page: 2 of 83, First Previous Next Last | Show Records Per Page |
- SCN2A
- SCN2B
- SCN3A
- SCN3B
- SCN4A
- SCN4A-related channelopathy
- SCN4A-related myopathy, autosomal recessive
- SCN4B
- SCN5A
- SCN8A
- SCN8A
- SCN9A
- SCN9A
- SCNM1
- SCNN1A
- SCNN1B
- SCNN1G
- SCO1
- SCO2
- SCP2
- SCUBE3
- SCYL1
- SCYL2
- SDC3
- SDCCAG8
- SDHA
- SDHAF1
- SDHAF2
- SDHB
- SDHC
- SDHD
- SDR9C7
- SEC23A
- SEC23B
- SEC24D
- SEC61A1
- SEC61A1 deficiency
- SEC61B
- SEC61B-related polycystic liver disease
- SEC63
- SECISBP2
- SEL1L
- SELE
- SELENBP1
- SELENOI
- SELENON
- SELENON-related myopathy
- SELENOP
- SELP
- SEMA3A
