adult-onset autosomal dominant demyelinating leukodystrophy
Human disease
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adult-onset autosomal dominant demyelinating leukodystrophy
Summary
adult-onset autosomal dominant demyelinating leukodystrophy is a developmental defect during embryogenesis[1].
Key Facts
- adult-onset autosomal dominant demyelinating leukodystrophy's instance of is recorded as developmental defect during embryogenesis[2].
- adult-onset autosomal dominant demyelinating leukodystrophy's instance of is recorded as rare disease[3].
- adult-onset autosomal dominant demyelinating leukodystrophy's instance of is recorded as class of disease[4].
- adult-onset autosomal dominant demyelinating leukodystrophy is a type of leukodystrophy[5].
- adult-onset autosomal dominant demyelinating leukodystrophy is a type of abnormal eye movements[6].
- adult-onset autosomal dominant demyelinating leukodystrophy is a type of partial trisomy of the long arm of chromosome 5[7].
- adult-onset autosomal dominant demyelinating leukodystrophy is a type of autosomal dominant disease[8].
- adult-onset autosomal dominant demyelinating leukodystrophy's genetic association is recorded as LMNB1[9].
- adult-onset autosomal dominant demyelinating leukodystrophy's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060785[10].
- adult-onset autosomal dominant demyelinating leukodystrophy's exact match is recorded as http://identifiers.org/doid/DOID:0060785[11].
- adult-onset autosomal dominant demyelinating leukodystrophy's on focus list of Wikimedia project is recorded as WikiProject Medicine[12].