Mondo Disease Ontology
5883 terms(s) returned
| Term Type: | Record: 4951 to 5000 of 5883 Records | Page: 100 of 118, First Previous Next Last | Show Records Per Page |
- 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
- progressive myoclonic epilepsy type 7
- progressive myoclonic epilepsy type 8
- progressive myoclonic epilepsy type 9
- progressive myoclonic epilepsy with dystonia
- progressive myoclonus epilepsy
- progressive myopathy, non-human animal
- progressive myopathy, pig
- progressive neuronopathy, dog
- progressive neuronopathy, non-human animal
- 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
- progressive retinal atrophy, BBS4-related, dog
- progressive retinal atrophy, CCDC66 related, dog
- progressive retinal atrophy, CNGA1-related, dog
- progressive retinal atrophy, CNGB1-related, dog
- progressive retinal atrophy, FAM161A-related, dog
