×
×
PubCaseFinder
About
Datasets
History
Terms
RDF
API
Contact
EN
/
JA
WAGR syndrome
A rare genetic disorder characterized by an unusual complex of congenital developmental abnormalities with intellectual disability, and an increased risk of developing Wilms tumor.
Micrognathia
Developmental hypoplasia of the mandible.
Total:
0
20
40
60
100
(per page)
PMID (PMCID)