Mondo Disease Ontology
52588 terms(s) returned
| Term Type: Class | Record: 45001 to 45050 of 52588 Records | Page: 901 of 1052, First Previous Next Last | Show Records Per Page |
- progressive bifocal chorioretinal atrophy
- progressive bulbar palsy
- progressive bulbar palsy of childhood
- progressive cavitating leukoencephalopathy
- progressive deafness with stapes fixation
- progressive dementia with neuroserpin inclusion bodies
- progressive demyelinating neuropathy with bilateral striatal necrosis
- progressive encephalomyelitis with rigidity
- progressive encephalomyelitis with rigidity and myoclonus
- 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 IB
- progressive familial heart block type II
- 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 atrophy
- progressive muscular dystrophy
- progressive myoclonic epilepsy type 3
- progressive myoclonic epilepsy type 6
- progressive myoclonic epilepsy type 7
- progressive myoclonic epilepsy type 8
- progressive myoclonic epilepsy type 9
- progressive myoclonic epilepsy with dystonia
- progressive myoclonus epilepsy
- progressive nodular histiocytosis
- progressive non-fluent aphasia
- progressive non-infectious anterior vertebral fusion
- progressive osseous heteroplasia
- progressive peripheral pterygium
- progressive pseudorheumatoid arthropathy of childhood
- progressive relapsing multiple sclerosis
