×
×
PubCaseFinder
About
Datasets
History
Terms
RDF
API
Contact
EN
/
JA
Trichorhinophalangeal syndrome type 2
A very rare, genetic, multiple congenital anomaly disorder characterized by bone abnormalities, distinctive facial features, multiple exostoses, and intellectual disability.
Aplasia/Hypoplasia of the mandible
Absence or underdevelopment of the mandible.
Total:
0
20
40
60
100
(per page)
PMID (PMCID)