familial partial lipodystrophy Disease Ontology Browser

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Disease Ontology Browser

familial partial lipodystrophy (DOID:0050440)
Alliance: disease page
Synonyms: Dunnigan Syndrome; Koberling-Dunnigan Syndrome
Alt IDs: MESH:D052496, NCI:C165527, NCI:C84708, OMIM:PS151660, ORDO:98306, UMLS_CUI:C0271694, UMLS_CUI:C1720859, UMLS_CUI:C1720860, UMLS_CUI:C1720861
Definition: A partial lipodystrophy characterized by abnormal subcutaneous adipose tissue distribution beginning in late childhood or early adult life.

Disease References using Mouse Models (4)

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Allelic Composition	Genetic Background	Reference	Phenotypes
Ppargtm2(tTA)Yba/Pparg+	involves: 129S1/SvImJ * C57BL/6	J:125992	View
Ppargtm3(tTA)Yba/Pparg+	involves: 129S1/SvImJ * C57BL/6	J:125992	View
Lepob/Lepob Ppargtm1Avp/Pparg+	involves: 129S2/SvPas * C57BL/6	J:116568	View

Allelic Composition	Genetic Background	Reference	Phenotypes
Ppargtm1Rev/Pparg+	involves: 129S4/SvJae * C57BL/6J	J:60354	View
Ppargtm1Mae/Pparg+	involves: 129S6/SvEvTac * C57BL/6	J:91362	View
Ppargtm1Avp/Pparg+	involves: 129S2/SvPas * C57BL/6	J:116568	View

Allelic Composition	Genetic Background	Reference	Phenotypes
Zmpste24tm1Otin/Zmpste24tm1Otin	involves: 129P2/Ola * C57BL/6	J:76209	View

Allelic Composition	Genetic Background	Reference	Phenotypes
Lmnatm1Stw/Lmnatm1Stw	involves: 129S1/Sv * C57BL/6J	J:75101	View
Lmnatm1Stw/Lmna+	involves: 129S1/Sv * C57BL/6J	J:75101	View

Allelic Composition	Genetic Background	Reference	Phenotypes
Tg(Fabp4-LMNA*R482Q)11ACdl/0	FVB-Tg(Fabp4-LMNA*R482Q)11ACdl	J:149858	View