← Назад
🧬

CRPPA

CDP-L-ribitol pyrophosphorylase A

gene with protein productOMIM: 6146314 заболевания
GeneCards ↗Open Targets ↗NCBI Gene ↗OMIM ↗

Ассоциированные заболевания

Disease-causing germline mutation(s) (loss of function) in3
Congenital muscular dystrophy without intellectual disabilityORPHA:370980
→
ISPD-related limb-girdle muscular dystrophy R20ORPHA:352479
→
Walker-Warburg syndromeORPHA:899
→
Герминативная мутация (причина)1
Muscle-eye-brain diseaseORPHA:588
→
Данные: Orphadata (CC-BY-4.0)