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Disease association ontology term - MONDO:0015905 - syndromic dyslipidemia

Term summary

ID
MONDO:0015905
Name
syndromic dyslipidemia
Ontology or CV name
Disease association
Definition
A inherited lipid metabolism disorder that is part of a larger syndrome.

Parents

Annotation

Disease association

MONDO:0009025 - apparent mineralocorticoid excess

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Genes:

MONDO:0010621 - CHILD syndrome

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Genes:

MONDO:0010221 - CHIME syndrome

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Genes:

MONDO:0019149 - cholesteryl ester storage disease

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Genes:

MONDO:0013760 - congenital ichthyosis-intellectual disability-spastic quadriplegia syndrome

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Genes:

MONDO:0012787 - hereditary spastic paraplegia 39

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Genes:

MONDO:0009849 - hyperimmunoglobulinemia D with periodic fever

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Genes:

MONDO:0009398 - hyperphosphatasia with intellectual disability syndrome 1

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MONDO:0013882 - hyperphosphatasia with intellectual disability syndrome 2

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MONDO:0014318 - hyperphosphatasia with intellectual disability syndrome 4

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MONDO:0014457 - hyperphosphatasia with intellectual disability syndrome 5

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MONDO:0014780 - hyperphosphatasia with intellectual disability syndrome 6

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MONDO:0014832 - intellectual disability, autosomal recessive 53

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MONDO:0012481 - mevalonic aciduria

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Genes:

MONDO:0010466 - multiple congenital anomalies-hypotonia-seizures syndrome 2

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MONDO:0008972 - rhizomelic chondrodysplasia punctata type 1

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Genes:

MONDO:0014743 - rhizomelic chondrodysplasia punctata type 5

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MONDO:0020747 - sitosterolemia 1

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MONDO:0020748 - sitosterolemia 2

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MONDO:0010035 - Smith-Lemli-Opitz syndrome

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MONDO:0019148 - Wolman disease

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