Mondo Disease Ontology
5650 terms(s) returned
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- progressive ataxia, cattle
- progressive ataxia, dog
- progressive ataxia, non-human animal
- progressive ataxia, pig
- progressive atraumatic breakdown of the hindlimb suspensory ligament, non-human animal
- progressive axonopathy, dog
- progressive axonopathy, non-human animal
- progressive bifocal chorioretinal atrophy
- progressive bulbar palsy
- progressive bulbar palsy of childhood
- progressive cavitating leukoencephalopathy
- progressive cerebellar abiotrophy, non-human animal
- progressive cerebellar abiotrophy, pig
- progressive deafness with stapes fixation
- progressive degenerative myeloencephalopathy, PNPLA8-related, cattle
- progressive degenerative myeloencephalopathy, PNPLA8-related, dog
- progressive dementia with neuroserpin inclusion bodies
- progressive demyelinating neuropathy with bilateral striatal necrosis
- progressive early-onset cerebellar ataxia, SEL1L-related, dog
- 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 hypotonia-intellectual disability-facial dysmorphism syndrome due to FYVE-defective RBSN
- 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
