Experimental Factor Ontology
94474 terms(s) returned
| Term Type: | Record: 83451 to 83500 of 94474 Records | Page: 1670 of 1890, First Previous Next Last | Show Records Per Page |
- progranulin
- progranulin (human)
- progranulin measurement
- progranulin proteolytic cleavage product
- progranulin, signal peptide removed form
- progranulin, signal peptide removed form (human)
- progression free survival
- progressive bifocal chorioretinal atrophy
- progressive bulbar palsy
- progressive bulbar palsy of childhood
- progressive cavitating leukoencephalopathy
- progressive cerebello-cerebral atrophy
- progressive deafness with stapes fixation
- progressive demyelinating neuropathy with bilateral striatal necrosis
- progressive encephalopathy with leukodystrophy due to DECR deficiency
- progressive essential tremor-speech impairment-facial dysmorphism-intellectual disability-abnormal behavior syndrome
- progressive external ophthalmoplegia
- progressive external ophthalmoplegia with mitochondrial DNA deletions
- progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1
- progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 2
- progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 3
- progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 4
- progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 5
- progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 1
- progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 2
- progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 3
- progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 4
- progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 5
- progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal recessive 6
- progressive familial heart block
- progressive familial heart block, type 1A
- progressive familial intrahepatic cholestasis
- progressive familial intrahepatic cholestasis type 1
- progressive familial intrahepatic cholestasis type 2
- progressive familial intrahepatic cholestasis type 3
- progressive microcephaly-seizures-cortical blindness-developmental delay syndrome
- progressive multifocal leukoencephalopathy
- progressive muscular dystrophy
- progressive myoclonic epilepsy type 3
- progressive myoclonic epilepsy type 6
- progressive myoclonic epilepsy type 9
- progressive myoclonic epilepsy with dystonia
- progressive myoclonus epilepsy
- progressive non-fluent aphasia
- progressive non-infectious anterior vertebral fusion
- progressive osseous heteroplasia
- progressive pseudorheumatoid arthropathy of childhood
- progressive retinal dystrophy due to retinol transport defect
- progressive scapulohumeroperoneal distal myopathy
- progressive sensorineural hearing loss-hypertrophic cardiomyopathy syndrome
