8p11.2 deletion syndrome
MONDO:00166578p11.2 deletion syndrome is a contiguous gene syndrome characterized by the association of congenital spherocytosis, dysmorphic features, growth delay and hypogonadotropic hypogonadism.
Also known as: Del(8)(p11.2), monosomy 8p11.2
2 clinical trials for this condition and its sub-types.
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Disease
(618)
Human disease
(14)
Chromosomal disorder
(12)
Disease of genetic or genomic mechanism
(2)
Autosomal anomaly
(0)
Chromosome 8 disorder
(0)
Disease by etiologic mechanism
(0)
Partial deletion of chromosome 8
(0)
Partial deletion of the short arm of chromosome 8
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Syndrome caused by partial chromosomal deletion
(0)