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Up to: Syndromic disease · Inherited lipid metabolism disorder

Syndromic dyslipidemia

A inherited lipid metabolism disorder that is part of a larger syndrome.

0 trials tagged with this condition →

CHILD syndrome 37 trials
Smith-Lemli-Opitz syndrome 6 trials
Cerebrotendinous xanthomatosis 6 trials
Familial lipoprotein lipase deficiency 6 trials
Lysosomal acid lipase deficiency 4 trials · 6 incl. sub-types Sub-types →
Barth syndrome 5 trials
Mevalonate kinase deficiency 3 trials · 4 incl. sub-types Sub-types →
GM1 gangliosidosis type 1 3 trials
Sjogren-Larsson syndrome 3 trials
Nephrotic syndrome 14 3 trials
Apparent mineralocorticoid excess 1 trial
Neuronal ceroid lipofuscinosis 8 northern epilepsy variant 1 trial
Rhizomelic chondrodysplasia punctata type 1 1 trial
Peroxisome biogenesis disorder due to PEX5 defect in the PEX7-binding domain 0 trials · 1 incl. sub-types Sub-types →
CHIME syndrome 0 trials
Krabbe disease due to saposin A deficiency 0 trials
PHARC syndrome 0 trials
Autosomal recessive complex spastic paraplegia due to kennedy pathway dysfunction 0 trials
Congenital ichthyosis-intellectual disability-spastic quadriplegia syndrome 0 trials
Familial apolipoprotein C-II deficiency 0 trials
Fatty acid hydroxylase-associated neurodegeneration 0 trials
Hereditary spastic paraplegia 39 0 trials Sub-types →
Hyperlipoproteinemia, type 1D 0 trials
Hyperphosphatasia-intellectual disability syndrome 0 trials Sub-types →
Intellectual disability, autosomal recessive 53 0 trials
Lipoprotein glomerulopathy 0 trials
Multiple congenital anomalies-hypotonia-seizures syndrome 2 0 trials
Sea-blue histiocyte syndrome 0 trials
Sitosterolemia 0 trials Sub-types →