Abnormality of lipid metabolism
Symptom Information:
Symptom ID: | HPO:0003119 | ||||||||||||||||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): | |||||||||||||||||||||||||
Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of metabolism/homeostasis(HPO:0001939) Abnormality of lipid metabolism(HPO:0003119) MedDRA: Metabolism and nutrition disorders(MedDRA:10027433) Abnormality of lipid metabolism(HPO:0003119) Congenital, familial and genetic disorders(MedDRA:10010331) Metabolic and nutritional disorders congenital(MedDRA:10027424) Abnormality of lipid metabolism(HPO:0003119) |
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Database Frequency: | 60 / 7739 | ||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
19p13.12 microdeletion syndrome | (Orphanet:254346) |
Acute intermittent porphyria | (Orphanet:79276) |
Adult Still's disease | (Orphanet:829) |
Alström syndrome | (Orphanet:64) |
Apolipoprotein A-I deficiency | (Orphanet:425) |
Bardet-Biedl syndrome 10 | (OMIM:615987) |
Bardet-Biedl syndrome 12 | (OMIM:615989) |
Bardet-Biedl syndrome 5 | (OMIM:615983) |
Bardet-Biedl syndrome 6 | (OMIM:605231) |
Berardinelli-Seip congenital lipodystrophy | (Orphanet:528) |
Bietti crystalline dystrophy | (Orphanet:41751) |
Carnitine palmitoyl transferase 1A deficiency | (Orphanet:156) |
Cerebrotendinous xanthomatosis | (Orphanet:909) |
Cholestasis - lymphedema | (Orphanet:1414) |
Cushing syndrome | (Orphanet:553) |
Fabry disease | (Orphanet:324) |
Familial LCAT deficiency | (Orphanet:79293) |
Familial partial lipodystrophy associated with PPARG mutations | (Orphanet:79083) |
Familial partial lipodystrophy due to AKT2 mutations | (Orphanet:79085) |
Familial partial lipodystrophy, Dunnigan type | (Orphanet:2348) |
GM1 gangliosidosis | (Orphanet:354) |
Glycogen storage disease due to glucose-6-phosphatase deficiency | (Orphanet:364) |
Glycogen storage disease due to glycogen debranching enzyme deficiency | (Orphanet:366) |
Glycogen storage disease due to phosphorylase kinase deficiency | (Orphanet:370) |
Griscelli disease | (Orphanet:381) |
Griscelli disease type 1 | (Orphanet:79476) |
Griscelli disease type 2 | (Orphanet:79477) |
Growth hormone insensitivity syndrome | (Orphanet:181393) |
Hypoalphalipoproteinemia | (Orphanet:31153) |
Kennedy disease | (Orphanet:481) |
LCAT deficiency | (Orphanet:650) |
LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 5 | (OMIM:615238) |
LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 6 | (OMIM:615980) |
Laron syndrome | (Orphanet:633) |
Lipodystrophy due to peptidic growth factors deficiency | (Orphanet:1979) |
Mandibuloacral dysplasia | (Orphanet:2457) |
Mandibuloacral dysplasia with type A lipodystrophy | (Orphanet:90153) |
Mandibuloacral dysplasia with type B lipodystrophy | (Orphanet:90154) |
Maternally-inherited diabetes and deafness | (Orphanet:225) |
Maturity-onset diabetes of the young, type 2 | (OMIM:125851) |
Megalocornea-intellectual deficit syndrome | (Orphanet:2479) |
Metachromatic leukodystrophy | (Orphanet:512) |
Mucolipidosis type 2 | (Orphanet:576) |
Mucolipidosis type 4 | (Orphanet:578) |
Neonatal intrahepatic cholestasis due to citrin deficiency | (Orphanet:247598) |
Nephrosis - deafness - urinary tract - digital malformations | (Orphanet:2669) |
Neutral lipid storage disease | (Orphanet:165) |
Oculocerebrorenal syndrome | (Orphanet:534) |
Partial acquired lipodystrophy | (Orphanet:79087) |
Primary lipodystrophy | (Orphanet:90970) |
Progeria - short stature - pigmented nevi | (Orphanet:2959) |
Retinohepatoendocrinologic syndrome | (Orphanet:3087) |
Sialidosis type 1 | (Orphanet:812) |
Smith-Lemli-Opitz syndrome | (Orphanet:818) |
Smith-Magenis syndrome | (Orphanet:819) |
Stiff skin syndrome | (Orphanet:2833) |
Subaortic stenosis - short stature | (Orphanet:3191) |
Tay-Sachs disease | (Orphanet:845) |
Uhl anomaly | (Orphanet:3403) |
Williams syndrome | (Orphanet:904) |