← Назад
🧬

HESX1

HESX homeobox 1

gene with protein productOMIM: 6018025 заболеваний
GeneCards ↗Open Targets ↗NCBI Gene ↗OMIM ↗

Ассоциированные заболевания

Герминативная мутация (причина)5
Septo-optic dysplasia spectrumORPHA:3157
→
Kallmann syndromeORPHA:478
→
Hypothyroidism due to deficient transcription factors involved in pituitary development or functionORPHA:226307
→
Pituitary stalk interruption syndromeORPHA:95496
→
Combined pituitary hormone deficiencies, genetic formsORPHA:95494
→
Данные: Orphadata (CC-BY-4.0)