Disease #03919 (MDPL (hypoplasia, mandibular, deafness, progeroid features, and lipodystrophy syndrome (MDPL)), OMIM:615381)

Official abbreviation MDPL
Name hypoplasia, mandibular, deafness, progeroid features, and lipodystrophy syndrome (MDPL)
OMIM ID 615381
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene POLD1
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Disease features -
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Individuals

1 entry on 1 page. Showing entry 1.
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00038583 - - - - - - - - 0 - - MDPL - POLD1 POLD1 2 1 Davor Lessel
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