← Назад
🧬
PCNT
pericentrin
gene with protein product
OMIM: 605925
2 заболевания
GeneCards ↗
Open Targets ↗
NCBI Gene ↗
OMIM ↗
Ассоциированные заболевания
Ген-кандидат
1
Seckel syndrome
ORPHA:808
→
Disease-causing germline mutation(s) (loss of function) in
1
Microcephalic osteodysplastic primordial dwarfism type II
ORPHA:2637
→
Home
Calc.
Tools
Sign in
MEDLIB
Home
Tools
Pricing
Sign in
Language
ҚАЗ
EN
DE
RU
Главная
Инструменты
Редкие заболевания
PCNT
🧬
PCNT
pericentrin
gene with protein product
OMIM: 605925
2 заболевания
GeneCards ↗
Open Targets ↗
NCBI Gene ↗
OMIM ↗
Ассоциированные заболевания
Ген-кандидат
1
Seckel syndrome
ORPHA:808
→
Disease-causing germline mutation(s) (loss of function) in
1
Microcephalic osteodysplastic primordial dwarfism type II
ORPHA:2637
→