partial lipodystrophy, congenital cataracts, and neurodegeneration syndrome
MONDO:0011714Mondo
Findings
No curated finding names partial lipodystrophy, congenital cataracts, and neurodegeneration syndrome yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
- Inheritance
- Autosomal dominant inheritance
- Onset and course
- Congenital onset · Neonatal onset · Young adult onset
HPO, annotations 2026-09-02
Features
48 features
What the disease is reported to present with, and how often among people who have it — never how often a feature means the disease. HPO, annotations 2026-09-02.
- Cutis marmorataHPOHP:0000965
- 2 of 2 reported patients
- HypertriglyceridemiaHPOHP:0002155
- 3 of 3 reported patients
- Triangular faceHPOHP:0000325
- 2 of 2 reported patients
- LipodystrophyHPOHP:0009125
- 4 of 5 reported patients
- Acanthosis nigricansHPOHP:0000956
- 2 of 3 reported patients
- Developmental cataractHPOHP:0000519
- 2 of 3 reported patients
- Distal sensory impairmentHPOHP:0002936
- 2 of 3 reported patients
- DysdiadochokinesisHPOHP:0002075
- 2 of 3 reported patients
- Lower limb muscle weaknessHPOHP:0007340
- 2 of 3 reported patients
- Pigmentary retinopathyHPOHP:0000580
- 2 of 3 reported patients
- Recurrent pancreatitisHPOHP:0100027
- 2 of 3 reported patients
- Type I diabetes mellitusHPOHP:0100651
- 2 of 3 reported patients · Young adult onset
Show the remaining 36
- CataractHPOHP:0000518
- 1 of 2 reported patients
- DiarrheaHPOHP:0002014
- 1 of 2 reported patients
- Dry skinHPOHP:0000958
- 1 of 2 reported patients
- DysphagiaHPOHP:0002015
- 1 of 2 reported patients
- Facial wrinklingHPOHP:0009762
- 1 of 2 reported patients
- Failure to thriveHPOHP:0001508
- 1 of 2 reported patients
Genes
1 gene
Germline variants in the gene encoding each protein, as classified by GenCC submitters, each in their own words. Limited, disputed and refuted submissions are listed too.
- CAV1HGNC:1527
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal dominant · 2020
Where it sits
- A kind of
Other names
1 name
Resolves to: partial lipodystrophy, congenital cataracts, and neurodegeneration syndrome
- Also called
- lipodystrophy, familial partial, type 7