congenital generalized lipodystrophy type 3

Summary
Synonym
  • Berardinelli-Seip congenital lipodystrophy type 3
Definition
A congenital generalized lipodystrophy that has_material_basis_in an autosomal recessive mutation of CAV1 on chromosome 7q31.2.
Super Class
congenital generalized lipodystrophy
External Links
Disease Ontology
DOID:0111137
Mondo Disease Ontology
OMIM
WikiPathways (from TogoID)
Related Genes
Displaying entries 11 - 20 of 28 in total
Gene ID Gene Symbol Description Source
5290 PIK3CA phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha
5291 PIK3CB phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta
5293 PIK3CD phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta
5294 PIK3CG phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma
5373 PMM2 phosphomannomutase 2
6319 SCD stearoyl-CoA desaturase
6389 SDHA succinate dehydrogenase complex flavoprotein subunit A
9663 LPIN2 lipin 2
10038 PARP2 poly(ADP-ribose) polymerase 2
10554 AGPAT1 1-acylglycerol-3-phosphate O-acyltransferase 1
The Human Phenotype Ontology
Displaying entries 21 - 30 of 36 in total
HPO ID HPO Term
HP:0000303 Mandibular prognathia
HP:0003712 Skeletal muscle hypertrophy
HP:0001015 Prominent superficial veins
HP:0009125 Lipodystrophy
HP:0001394 Cirrhosis
HP:0000855 Insulin resistance
HP:0002162 Low posterior hairline
HP:0011407 Proportionate tall stature
HP:0001249 Intellectual disability
HP:0008665 Clitoral hypertrophy
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: August 19, 2024