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PRRX1
paired related homeobox 1
gene with protein product
OMIM: 167420
1 заболевание
GeneCards ↗
Open Targets ↗
NCBI Gene ↗
OMIM ↗
Ассоциированные заболевания
Disease-causing germline mutation(s) (loss of function) in
1
Agnathia-holoprosencephaly-situs inversus syndrome
ORPHA:990
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Редкие заболевания
PRRX1
🧬
PRRX1
paired related homeobox 1
gene with protein product
OMIM: 167420
1 заболевание
GeneCards ↗
Open Targets ↗
NCBI Gene ↗
OMIM ↗
Ассоциированные заболевания
Disease-causing germline mutation(s) (loss of function) in
1
Agnathia-holoprosencephaly-situs inversus syndrome
ORPHA:990
→