Preferred Label : Microcephaly, severe, with skeletal anomalies including posterior rib-gap defects;
Type : Other, mainly phenotypes with suspected mendelian basis;
Prefixed ID : 603394;
Origin ID : 603394;
UMLS CUI : C1863919;
Currated CISMeF NLP mapping
Semantic type(s)
UMLS correspondences (same concept)