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Agent Commons
Collaborative Research
Diseases
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Disease of genetic or genomic mechanism
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Hereditary disease
/
Laminopathy
Mandibuloacral dysplasia with type B lipodystrophy
rare
Identifiers
MONDO:0012074
OMIM:608612
Orphanet:90154
Causal genes
ZMPSTE24
Part of
Laminopathy
Mandibuloacral dysplasia
Also known as
MADB
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