Disease #01496 (ADLD (leukodystrophy, adult-onset, autosomal dominant), OMIM:169500)

Official abbreviation ADLD
Name leukodystrophy, adult-onset, autosomal dominant
OMIM ID 169500
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 6
Phenotype entries for this disease 6
Associated with 1 gene LMNB1
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2020-09-19 21:03:07 +02:00 (CEST)


Individuals

6 entries on 1 page. Showing entries 1 - 6.
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00228220 - - 2-generation family, 3 affecteds - no United States - - - - - ADLD - MARCH3 LMNB1, MARCH3 1 30 LOVD
00228221 - - 4-generation family, 16 affecteds - no United States Irish - - - - ADLD - MARCH3 LMNB1, MARCH3 1 16 LOVD
00228222 - - 5-generation family, 30 affecteds - no United States Irish - - - - ADLD - MARCH3 LMNB1, MARCH3 1 30 LOVD
00228223 - - 3-generation family, 7 affecteds and 1 asymptomatic carrier (young) - no United States - - - - - ADLD - MARCH3 LMNB1, MARCH3 2 7 LOVD
00228224 - Giorgio et al., 2013 Human Mutation - - no - - - - - - ADLD adult onset demyelination LMNB1 LMNB1, MARCH3 1 1 Quasar Padiath
00228225 - - - - no - - - - - - ADLD adult onset demyelination LMNB1 LMNB1, MARCH3 1 1 Quasar Padiath
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