×
×
PubCaseFinder
About
Datasets
History
Terms
RDF
API
Contact
EN
/
JA
8p11.2 deletion syndrome
8p11.2 deletion syndrome is a contiguous gene syndrome characterized by the association of congenital spherocytosis, dysmorphic features, growth delay and hypogonadotropic hypogonadism.
Splenomegaly
Abnormal increased size of the spleen.
合計:
0
20
40
60
100
(表示件数)
PMID (PMCID)