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PROP1

PROP paired-like homeobox 1

gene with protein productOMIM: 6015383 заболевания
GeneCards ↗Open Targets ↗NCBI Gene ↗OMIM ↗

Ассоциированные заболевания

Герминативная мутация (причина)3
Hypothyroidism due to deficient transcription factors involved in pituitary development or functionORPHA:226307
→
Non-acquired panhypopituitarismORPHA:90695
→
Combined pituitary hormone deficiencies, genetic formsORPHA:95494
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Данные: Orphadata (CC-BY-4.0)