Mondo Disease Ontology
1825 terms(s) returned
| Term Type: | Record: 1051 to 1100 of 1825 Records | Page: 22 of 37, First Previous Next Last | Show Records Per Page |
- leukodystrophy, adult-onset, autosomal dominant, without amyloid angiopathy
- leukodystrophy, childhood-onset, remitting
- leukodystrophy, demyelinating, adult-onset
- leukodystrophy, demyelinating, adult-onset, autosomal dominant, atypical
- leukodystrophy, demyelinating, adult-onset, autosomal dominant, typical
- leukodystrophy, dog
- leukodystrophy, hypomyelinating, 14
- leukodystrophy, hypomyelinating, 15
- leukodystrophy, hypomyelinating, 16
- leukodystrophy, hypomyelinating, 17
- leukodystrophy, hypomyelinating, 18
- leukodystrophy, hypomyelinating, 19, transient infantile
- leukodystrophy, hypomyelinating, 20
- leukodystrophy, hypomyelinating, 21
- leukodystrophy, hypomyelinating, 22
- leukodystrophy, hypomyelinating, 23, with ataxia, deafness, liver dysfunction, and dilated cardiomyopathy
- leukodystrophy, hypomyelinating, 24
- leukodystrophy, hypomyelinating, 25
- leukodystrophy, hypomyelinating, 26, with chondrodysplasia
- leukodystrophy, hypomyelinating, 27
- leukodystrophy, hypomyelinating, 28
- leukodystrophy, hypomyelinating, 7, with or without oligodontia and/or hypogonadotropic hypogonadism
- leukodystrophy, non-human animal
- leukodystrophy, sheep
- leukoencephalomyelopathy, dog
- leukoencephalomyelopathy, non-human animal
- leukoencephalopathy with bilateral anterior temporal lobe cysts
- leukoencephalopathy with brain stem and spinal cord involvement-high lactate syndrome
- leukoencephalopathy with calcifications and cysts
- leukoencephalopathy with mild cerebellar ataxia and white matter edema
- leukoencephalopathy with vanishing white matter
- leukoencephalopathy with vanishing white matter 1
- leukoencephalopathy with vanishing white matter 2
- leukoencephalopathy with vanishing white matter 3
- leukoencephalopathy with vanishing white matter 4
- leukoencephalopathy with vanishing white matter 5
- leukoencephalopathy, acute reversible, with increased urinary alpha-ketoglutarate
- leukoencephalopathy, arthritis, colitis, and hypogammaglobulinema
- leukoencephalopathy, developmental delay, and episodic neurologic regression syndrome
- leukoencephalopathy, diffuse hereditary, with spheroids 1
- leukoencephalopathy, hereditary diffuse, with spheroids
- leukoencephalopathy, hereditary diffuse, with spheroids 2
- leukoencephalopathy, megalencephalic
- leukoencephalopathy, motor delay, spasticity, and dysarthria syndrome
- leukoencephalopathy, porphyria-related
- leukoencephalopathy, progressive, infantile-onset, with or without deafness
- leukoencephalopathy, progressive, with ovarian failure
- leukoencephalopathy-palmoplantar keratoderma syndrome
- leukoencephalopathy-thalamus and brainstem anomalies-high lactate syndrome
- leukonychia totalis
