congenital generalized lipodystrophy type 4

Summary
Synonym
  • Berardinelli-Seip congenital lipodystrophy type 4 with muscular dystrophy
  • congenital generalised lipodystrophy type 4
  • generalised congenital lipodystrophy type 4
  • generalised congenital lipodystrophy with myopathy
  • generalized congenital lipodystrophy type 4
  • generalized congenital lipodystrophy with myopathy
Definition
A congenital generalized lipodystrophy that has_material_basis_in an autosomal recessive mutation of CAVIN1 on chromosome 17q21.2.
Super Class
congenital generalized lipodystrophy
Disease Ontology
DOID:0111138
Mondo Disease Ontology
ORDO
OMIM
GARD
MGI genotype (from TogoID)
WikiPathways (from TogoID)
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
284119 CAVIN1 caveolae associated protein 1
Displaying 1 entry
Gene ID Gene Symbol Description Source
19285 Cavin1 caveolae associated 1
The Human Phenotype Ontology
Displaying entries 1 - 10 of 36 in total
HPO ID HPO Term
HP:0000147 Polycystic ovaries
HP:0000294 Low anterior hairline
HP:0000141 Amenorrhea
HP:0000303 Mandibular prognathia
HP:0000158 Macroglossia
HP:0001639 Hypertrophic cardiomyopathy
HP:0001015 Prominent superficial veins
HP:0003712 Skeletal muscle hypertrophy
HP:0000855 Insulin resistance
HP:0002162 Low posterior hairline
Displaying 1 entry
Gene ID Gene Symbol Description
10555 AGPAT2 1-acylglycerol-3-phosphate O-acyltransferase 2

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 9, 2024