Experimental Factor Ontology
422 terms(s) returned
| Term Type: | Record: 1 to 50 of 422 Records | Page: 1 of 9, First Previous Next Last | Show Records Per Page |
- FADD-related immunodeficiency
- FASTKD2-related infantile mitochondrial encephalomyopathy
- FBLN1-related developmental delay-central nervous system anomaly-syndactyly syndrome
- FG syndrome 1
- FG syndrome 2
- FG syndrome 4
- FGFR3-related chondrodysplasia
- FHL1-related myopathy
- FLOTCH syndrome
- FLVCR1-related retinopathy with or without ataxia
- 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
- 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
- Filippi syndrome
- Fine-Lubinsky syndrome
- Finnish type amyloidosis
- Finnish upper limb-onset distal myopathy
- Floating-Harbor syndrome
- Flynn-Aird syndrome
- Fontaine progeroid syndrome
- Fowler syndrome
- Frank-Ter Haar syndrome
