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LHX3

LIM homeobox 3

gene with protein productOMIM: 6005772 заболевания
GeneCards ↗Open Targets ↗NCBI Gene ↗OMIM ↗

Ассоциированные заболевания

Герминативная мутация (причина)2
Hypothyroidism due to deficient transcription factors involved in pituitary development or functionORPHA:226307
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Non-acquired combined pituitary hormone deficiency-sensorineural hearing loss-spine abnormalities syndromeORPHA:231720
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Данные: Orphadata (CC-BY-4.0)