← Назад
🧬
MYT1L
myelin transcription factor 1 like
gene with protein product
OMIM: 613084
2 заболевания
GeneCards ↗
Open Targets ↗
NCBI Gene ↗
OMIM ↗
Ассоциированные заболевания
Роль в фенотипе
1
2p25.3 microduplication syndrome
ORPHA:699850
→
Disease-causing germline mutation(s) (loss of function) in
1
MYT1L-related developmental delay-intellectual disability-obesity syndrome
ORPHA:647799
→
Home
Calc.
Tools
Sign in
MEDLIB
Home
Tools
Pricing
Sign in
Language
ҚАЗ
EN
DE
RU
Главная
Инструменты
Редкие заболевания
MYT1L
🧬
MYT1L
myelin transcription factor 1 like
gene with protein product
OMIM: 613084
2 заболевания
GeneCards ↗
Open Targets ↗
NCBI Gene ↗
OMIM ↗
Ассоциированные заболевания
Роль в фенотипе
1
2p25.3 microduplication syndrome
ORPHA:699850
→
Disease-causing germline mutation(s) (loss of function) in
1
MYT1L-related developmental delay-intellectual disability-obesity syndrome
ORPHA:647799
→