Mondo Disease Ontology
1685 terms(s) returned
| Term Type: | Record: 101 to 150 of 1685 Records | Page: 3 of 34, First Previous Next Last | Show Records Per Page |
- FCHO1
- FCN3
- FCSK
- FDFT1
- FDPS
- FDX2
- FDXR
- FDXR
- FDXR-related optic atrophy mitochondrial dysfunction syndrome
- FECH
- FECH
- FEM1B
- FERMT1
- FERMT3
- FERMT3
- FERRY3
- FEZF1
- FEZF2
- FEZF2-related neurodevelopmental disorder
- FG syndrome
- FG syndrome 1
- FG syndrome 2
- FG syndrome 3
- FG syndrome 4
- FG syndrome 5
- FGA
- FGB
- FGD1
- FGD3
- FGD4
- FGD4
- FGF10
- FGF12
- FGF13
- FGF14
- FGF14
- FGF16
- FGF17
- FGF20
- FGF23
- FGF3
- FGF4
- FGF5
- FGF8
- FGF9
- FGFR1
- FGFR1-related Pfeiffer syndrome
- FGFR2
- FGFR2
- FGFR2-related Pfeiffer syndrome
