Preferred Label : Anemia, congenital hypoplastic, with multiple congenital anomalies/impaired intellectual
development syndrome;
Type : Other, mainly phenotypes with suspected mendelian basis;
Alternative titles and symbols : Anemia, congenital hypoplastic, with multiple congenital anomalies/mental retardation
syndrome;
Prefixed ID : 604315;
Origin ID : 604315;
UMLS CUI : C1858537;
Automatic exact mappings (from CISMeF team)
Semantic type(s)
UMLS correspondences (same concept)