Homozygous 11p15-P14 Deletion Syndrome

Alias:

Chromosome 11p15-P14 Deletion Syndrome

Hyperinsulinism, Infantile, with Enteropathy and Deafness

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Gene & Mutation

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References Literature

Homozygous 11p15-P14 Deletion Syndrome, is also known as chromosome 11p15-p14 deletion syndrome, and has symptoms including diarrhea and intractable vomiting. An important gene associated with Homozygous 11p15-P14 Deletion Syndrome is DEL11P15P14 (Chromosome 11p15-P14 Deletion Syndrome). Related phenotypes are failure to thrive and feeding difficulties in infancy

Related ID：

MALACARDS：HMZ004

OMIM：606528