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FGF8

fibroblast growth factor 8

gene with protein productOMIM: 6004838 заболеваний
GeneCards ↗Open Targets ↗NCBI Gene ↗OMIM ↗

Ассоциированные заболевания

Герминативная мутация (причина)6
Microform holoprosencephalyORPHA:280200
→
Septopreoptic holoprosencephalyORPHA:280195
→
Semilobar holoprosencephalyORPHA:220386
→
Midline interhemispheric variant of holoprosencephalyORPHA:93926
→
Lobar holoprosencephalyORPHA:93924
→
Alobar holoprosencephalyORPHA:93925
→
Disease-causing germline mutation(s) (loss of function) in2
Kallmann syndromeORPHA:478
→
Normosmic congenital hypogonadotropic hypogonadismORPHA:432
→
Данные: Orphadata (CC-BY-4.0)