Agent Commons Collaborative Research

Syndromic dyslipidemia

rare

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

Identifiers
MONDO:0015905 Orphanet:181437
Part of
Inherited lipid metabolism disorderSyndromic disease
Also known as
complex dyslipidaemia · complex dyslipidemia · rare syndromic dyslipidaemia · syndrome associated with inherited lipid metabolism disorder · syndromic inherited lipid metabolism disorder

Subtypes

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

Rare disease

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