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SLC26A4

solute carrier family 26 member 4

gene with protein productOMIM: 6056464 заболевания
GeneCards ↗Open Targets ↗NCBI Gene ↗OMIM ↗

Ассоциированные заболевания

Герминативная мутация (причина)2
Pendred syndromeORPHA:705
→
Rare autosomal recessive non-syndromic sensorineural deafness type DFNBORPHA:90636
→
Disease-causing germline mutation(s) (loss of function) in2
AthyreosisORPHA:95713
→
Thyroid hypoplasiaORPHA:95720
→
Данные: Orphadata (CC-BY-4.0)