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LHX4
LIM homeobox 4
gene with protein product
OMIM: 602146
4 заболевания
GeneCards ↗
Open Targets ↗
NCBI Gene ↗
OMIM ↗
Ассоциированные заболевания
Герминативная мутация (причина)
3
Hypothyroidism due to deficient transcription factors involved in pituitary development or function
ORPHA:226307
→
Short stature-pituitary and cerebellar defects-small sella turcica syndrome
ORPHA:85442
→
Pituitary stalk interruption syndrome
ORPHA:95496
→
Disease-causing germline mutation(s) (loss of function) in
1
Combined pituitary hormone deficiencies, genetic forms
ORPHA:95494
→
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Редкие заболевания
LHX4
🧬
LHX4
LIM homeobox 4
gene with protein product
OMIM: 602146
4 заболевания
GeneCards ↗
Open Targets ↗
NCBI Gene ↗
OMIM ↗
Ассоциированные заболевания
Герминативная мутация (причина)
3
Hypothyroidism due to deficient transcription factors involved in pituitary development or function
ORPHA:226307
→
Short stature-pituitary and cerebellar defects-small sella turcica syndrome
ORPHA:85442
→
Pituitary stalk interruption syndrome
ORPHA:95496
→
Disease-causing germline mutation(s) (loss of function) in
1
Combined pituitary hormone deficiencies, genetic forms
ORPHA:95494
→