Experimental Factor Ontology
1218 terms(s) returned
Term Type: Class | Record: 101 to 150 of 1218 Records | Page: 3 of 25, First Previous Next Last | Show Records Per Page |
- Familial hypocalciuric hypercalcemia type 2
- Familial hypocalciuric hypercalcemia type 3
- Familial intestinal malrotation - facial anomalies
- Familial isolated hypoparathyroidism
- Familial multinodular goiter
- Familial ocular anterior segment mesenchymal dysgenesis
- Familial osteochondritis dissecans
- Familial paroxysmal ataxia
- Familial partial lipodystrophy due to AKT2 mutations
- Familial partial lipodystrophy, Köbberling type
- Familial porphyria cutanea tarda
- Familial progressive cardiac conduction defect
- Familial prostate cancer
- Familial renal amyloidosis
- Familial renal amyloidosis due to Apolipoprotein AI variant
- Familial renal amyloidosis due to fibrinogen A alpha-chain variant
- Familial renal amyloidosis due to lysozyme variant
- Familial retinoblastoma
- Familial short QT syndrome
- Familial transthyretin-related amyloidosis
- Fanconi anemia
- Fanconi anemia complementation group A
- Fanconi anemia complementation group C
- Fanconi anemia complementation group D1
- Fanconi anemia complementation group D2
- Fanconi anemia complementation group E
- Fanconi anemia complementation group F
- Fanconi anemia complementation group G
- 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 group F protein
- Fanconi anemia, complementation group S
- Fanconi anemia, complementation group W
- Fanconi renotubular syndrome
- Fanconi renotubular syndrome 1
- Fanconi renotubular syndrome 2
- Farage
- Farber lipogranulomatosis
- Fas apoptotic inhibitory molecule 1
- Fasciitis
- Fascioliasis
- Fast-ATAC
- Fatal infantile lactic acidosis with methylmalonic aciduria