Term info
database cross reference
- MESH:D024182 (https://orcid.org/0000-0003-1967-3726)
- NCIT:C85215 (MONDO:equivalentTo)
created by
https://orcid.org/0000-0002-4142-7153
definition
A condition characterized by the inheritance of a chromosome pair from one parent and no chromosomal copies from the other parent. It results in developmental abnormalities or rare recessive disorders.
exactMatch
http://purl.obolibrary.org/obo/NCIT_C85215, http://identifiers.org/mesh/D024182
id
MONDO:0700086