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Coronary artery disease - hyperlipidemia - hypertension - diabetes - osteoporosis
1 OMIM reference -
1 associated gene
31 connected diseases
No signs/symptoms info
Disease Type of connection
Idiopathic juvenile osteoporosis
Osteogenesis imperfecta type 3
Osteogenesis imperfecta type 4
Berardinelli-Seip congenital lipodystrophy
Diffuse cutaneous systemic sclerosis
Heritable pulmonary arterial hypertension
Limited cutaneous systemic sclerosis
Young adult-onset Parkinsonism
Autosomal dominant nonsyndromic intellectual deficit
Craniopharyngioma
Desmoid tumor
Hepatocellular carcinoma, childhood-onset
Kufor-Rakeb syndrome
Parkinsonim due to ATP13A2 deficiency
Pilomatrixoma
Infantile systemic hyalinosis
Juvenile hyaline fibromatosis
Craniodiaphyseal dysplasia
Hyperostosis corticalis generalisata
Sclerosteosis
Familial capillary hemangioma
GAPO syndrome
Autosomal dominant Robinow syndrome
Niemann-Pick disease type C, adult neurologic onset
Niemann-Pick disease type C, juvenile neurologic onset
Niemann-Pick disease type C, late infantile neurologic onset
Niemann-Pick disease type C, severe early infantile neurologic onset
Niemann-Pick disease type C, severe perinatal form
Homozygous familial hypercholesterolemia
Alport syndrome - intellectual deficit - midface hypoplasia - elliptocytosis
Osteopathia striata - cranial sclerosis
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare cardiac disease
- Rare genetic disease
Classification (ICD10):
(no data available)
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: no data available
Average age of death: -
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
LRP6 O75581603507
No signs/symptoms info available.