Experimental Factor Ontology
440 terms(s) returned
| Term Type: | Record: 1 to 50 of 440 Records | Page: 1 of 9, First Previous Next Last | Show Records Per Page |
- FADD-related immunodeficiency
- FAM111A-related skeletal dysplasia
- FANCM Fanconi-like genomic instability disorder
- FASTKD2-related infantile mitochondrial encephalomyopathy
- FAT4-related neurodevelopmental disorder
- FBLN1-related developmental delay-central nervous system anomaly-syndactyly syndrome
- FDXR-related optic atrophy mitochondrial dysfunction syndrome
- FG syndrome 1
- FG syndrome 2
- FG syndrome 4
- FGFR1-related Pfeiffer syndrome
- FGFR2-related Pfeiffer syndrome
- FGFR3-related chondrodysplasia
- FHL1-related myopathy
- FLNB-associated autosomal dominant filamin related bone disorder
- FLOTCH syndrome
- FLVCR1-related retinopathy with or without ataxia
- FNIP1-associated syndrome
- FOXG1 disorder
- FRAXE intellectual disability
- FRAXF syndrome
- FZD4-related exudative vitreoretinopathy
- Fabry disease
- Fanconi anemia
- Fanconi anemia complementation group C
- Fanconi anemia complementation group D1
- Fanconi anemia complementation group D2
- Fanconi anemia complementation group E
- Fanconi anemia complementation group I
- Fanconi anemia complementation group J
- Fanconi anemia complementation group L
- Fanconi anemia complementation group N
- Fanconi anemia complementation group P
- Fanconi anemia complementation group Q
- Fanconi anemia complementation group R
- Fanconi anemia complementation group U
- Fanconi anemia complementation group V
- Fanconi anemia, complementation group S
- Fanconi anemia, complementation group W
- Fanconi renotubular syndrome
- Fanconi renotubular syndrome 1
- Fanconi renotubular syndrome 2
- Fanconi-like syndrome
- Farber lipogranulomatosis
- Faundes-Banka syndrome
- Feingold syndrome
- Feingold syndrome type 1
- Feingold syndrome type 2
- Ferguson-Bonni neurodevelopmental syndrome
- Fibulo-ulnar hypoplasia-renal anomalies syndrome
