Syndromic dyslipidemia
MONDO:0015905A inherited lipid metabolism disorder that is part of a larger syndrome.
Also known as: complex dyslipidaemia, complex dyslipidemia, syndrome associated with inherited lipid metabolism disorder, syndromic inherited lipid metabolism disorder, rare syndromic dyslipidaemia, rare syndromic dyslipidemia
73 clinical trials for this condition and its sub-types, 0 tagged with Syndromic dyslipidemia itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →Sub-types of Syndromic dyslipidemia
-
CHILD syndrome 37 trials
-
Smith-Lemli-Opitz syndrome 6 trials
-
Cerebrotendinous xanthomatosis 6 trials
-
Lysosomal acid lipase deficiency 4 trials · 6 incl. sub-types
2 sub-types
- Wolman disease 6 trials
- Cholesteryl ester storage disease 1 trial
-
Barth syndrome 5 trials
-
Mevalonate kinase deficiency 3 trials · 4 incl. sub-types
2 sub-types
- Hyperimmunoglobulinemia D with periodic fever 2 trials
- Mevalonic aciduria 0 trials
-
GM1 gangliosidosis type 1 3 trials
-
Sjogren-Larsson syndrome 3 trials
-
Nephrotic syndrome 14 3 trials
-
Peroxisome biogenesis disorder due to PEX5 defect in the PEX7-binding domain 0 trials · 1 incl. sub-types
1 sub-type
-
CHIME syndrome 0 trials
-
PHARC syndrome 0 trials
-
Hereditary spastic paraplegia 39 0 trials
1 sub-type
-
Hyperlipoproteinemia, type 1D 0 trials
-
6 sub-types
- Hyperphosphatasia with intellectual disability syndrome 1 0 trials
- Hyperphosphatasia with intellectual disability syndrome 2 0 trials
- Hyperphosphatasia with intellectual disability syndrome 3 0 trials
- Hyperphosphatasia with intellectual disability syndrome 4 0 trials
- Hyperphosphatasia with intellectual disability syndrome 5 0 trials
- Hyperphosphatasia with intellectual disability syndrome 6 0 trials
-
Lipoprotein glomerulopathy 0 trials
-
Sea-blue histiocyte syndrome 0 trials
-
Sitosterolemia 0 trials
2 sub-types
- Sitosterolemia 1 0 trials
- Sitosterolemia 2 0 trials
-
Gene therapy before birth: a new hope for babies with GM1 disease
Disease control Not yet recruitingThis early-stage trial tests giving a gene therapy to unborn babies diagnosed with GM1 gangliosidosis, a severe genetic disorder that damages the brain and body. The therapy uses a harmless virus to deliver a working copy of the missing enzyme gene. The main goal is to see if the…
Phase 1 • Sponsor: Tippi Mackenzie • Aim: Disease control
Last updated Sep 02, 2026 00:00 UTC
-
Could a simple gel boost gum healing in diabetes?
Disease control Not yet recruitingThis study tests whether adding hyaluronic acid gel to standard deep cleaning (scaling and root planing) improves gum healing in people with both diabetes and advanced gum disease. Twenty-three participants will receive the standard cleaning on all teeth, and then two gum pockets…
Sponsor: Marmara University • Aim: Disease control
Last updated Jun 27, 2026 13:05 UTC