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ENChromosome 1q41-Q42 Deletion Syndrome
Alias:
1q41q42 Microdeletion Syndrome
Monosomy 1q41q42
Del(1)(q41q42)
Chromosome Deletion Syndrome 1q41-Q42
1q41-Q42 Microdeletion Syndrome
Holoprosencephaly 10, Included
Holoprosencephaly 10
Hpe10, Included
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Chromosome 1q41-Q42 Deletion Syndrome, also known as 1q41q42 microdeletion syndrome, is related to wdr26-related intellectual disability and diaphragmatic hernia, congenital, and has symptoms including seizures An important gene associated with Chromosome 1q41-Q42 Deletion Syndrome is DEL1Q41Q42 (Chromosome 1q41-Q42 Deletion Syndrome). Affiliated tissues include heart and brain, and related phenotypes are intellectual disability and seizure
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