Disease #00889 (C syndrome, OMIM:211750)

Official abbreviation -
Name C syndrome
OMIM ID 211750
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene CD96
Associated tissues -
Disease features -
Remarks -

  Powered by LOVD v.3.0 Build 26
LOVD software ©2004-2021 Leiden University Medical Center 		There are currently no updates.