← Назад
🧬

RPL10

ribosomal protein L10

gene with protein productOMIM: 3121732 заболевания
GeneCards ↗Open Targets ↗NCBI Gene ↗OMIM ↗

Ассоциированные заболевания

Герминативная мутация (причина)1
X-linked intellectual disability-cerebellar hypoplasia-spondylo-epiphyseal dysplasia syndromeORPHA:459070
→
Disease-causing germline mutation(s) (loss of function) in1
X-linked microcephaly-growth retardation-prognathism-cryptorchidism syndromeORPHA:435938
→
Данные: Orphadata (CC-BY-4.0)