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LHX3
LIM homeobox 3
gene with protein product
OMIM: 600577
2 заболевания
GeneCards ↗
Open Targets ↗
NCBI Gene ↗
OMIM ↗
Ассоциированные заболевания
Герминативная мутация (причина)
2
Hypothyroidism due to deficient transcription factors involved in pituitary development or function
ORPHA:226307
→
Non-acquired combined pituitary hormone deficiency-sensorineural hearing loss-spine abnormalities syndrome
ORPHA:231720
→
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Редкие заболевания
LHX3
🧬
LHX3
LIM homeobox 3
gene with protein product
OMIM: 600577
2 заболевания
GeneCards ↗
Open Targets ↗
NCBI Gene ↗
OMIM ↗
Ассоциированные заболевания
Герминативная мутация (причина)
2
Hypothyroidism due to deficient transcription factors involved in pituitary development or function
ORPHA:226307
→
Non-acquired combined pituitary hormone deficiency-sensorineural hearing loss-spine abnormalities syndrome
ORPHA:231720
→