syndromic dyslipidemia

Findings

No curated finding names syndromic dyslipidemia yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.

Definition

Where it sits

A kind of

• inherited lipid metabolism disorder
• syndromic disease

Narrower terms (29)

• apparent mineralocorticoid excess
• autosomal recessive complex spastic paraplegia due to kennedy pathway dysfunction
• Barth syndrome
• cerebrotendinous xanthomatosis
• CHILD syndrome
• CHIME syndrome
• congenital ichthyosis-intellectual disability-spastic quadriplegia syndrome
• familial apolipoprotein C-II deficiency
• familial lipoprotein lipase deficiency
• fatty acid hydroxylase-associated neurodegeneration
• GM1 gangliosidosis type 1
• hereditary spastic paraplegia 39
• hyperlipoproteinemia, type 1D
• hyperphosphatasia-intellectual disability syndrome
• intellectual disability, autosomal recessive 53
• Krabbe disease due to saposin A deficiency
• lipoprotein glomerulopathy
• lysosomal acid lipase deficiency
• mevalonate kinase deficiency
• multiple congenital anomalies-hypotonia-seizures syndrome 2
• nephrotic syndrome 14
• neuronal ceroid lipofuscinosis 8 northern epilepsy variant
• peroxisome biogenesis disorder due to PEX5 defect in the PEX7-binding domain
• PHARC syndrome
• rhizomelic chondrodysplasia punctata type 1
• sea-blue histiocyte syndrome
• sitosterolemia
• Sjogren-Larsson syndrome
• Smith-Lemli-Opitz syndrome

Resolves to: syndromic dyslipidemia

Also called

complex dyslipidaemiacomplex dyslipidemiasyndrome associated with inherited lipid metabolism disordersyndromic inherited lipid metabolism disorder