Disease #01492

Official abbreviation PFMCCD
Name foramina, parietal, with cleidocranial dysplasia (PFMCCD)
OMIM ID 168550
Human Phenotype Ontology Project (HPO) HPO
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene MSX2
Associated tissues -
Disease features -
Remarks -