LRP5 — LDL receptor related protein 5 | MEDLIB

gene with protein productOMIM: 6035069 заболеваний

GeneCards ↗Open Targets ↗NCBI Gene ↗OMIM ↗

Ассоциированные заболевания

Герминативная мутация (причина)5

Endosteal hyperostosis, Worth typeORPHA:2790

Isolated polycystic liver diseaseORPHA:2924

Hyperostosis corticalis generalisataORPHA:3416

Familial exudative vitreoretinopathyORPHA:891

LRP5-related primary osteoporosisORPHA:498481

Disease-causing germline mutation(s) (gain of function) in2

Osteosclerosis-developmental delay-craniosynostosis syndromeORPHA:178377

Autosomal dominant osteopetrosis type 1ORPHA:2783

Основной фактор предрасположенности2

LRP5-related primary osteoporosisORPHA:498481

Retinopathy of prematurityORPHA:90050

Disease-causing germline mutation(s) (loss of function) in1

Osteoporosis-pseudoglioma syndromeORPHA:2788

gene with protein productOMIM: 6035069 заболеваний

GeneCards ↗Open Targets ↗NCBI Gene ↗OMIM ↗

Ассоциированные заболевания

Герминативная мутация (причина)5

Endosteal hyperostosis, Worth typeORPHA:2790

Isolated polycystic liver diseaseORPHA:2924

Hyperostosis corticalis generalisataORPHA:3416

Familial exudative vitreoretinopathyORPHA:891

LRP5-related primary osteoporosisORPHA:498481

Disease-causing germline mutation(s) (gain of function) in2

Osteosclerosis-developmental delay-craniosynostosis syndromeORPHA:178377

Autosomal dominant osteopetrosis type 1ORPHA:2783

Основной фактор предрасположенности2

LRP5-related primary osteoporosisORPHA:498481

Retinopathy of prematurityORPHA:90050

Disease-causing germline mutation(s) (loss of function) in1

Osteoporosis-pseudoglioma syndromeORPHA:2788