A holoprosencephaly that has material basis in variation in the chromosome region 2q37.1-q37.3. [ DOID:0110874 http://www.ncbi.nlm.nih.gov/pubmed/11343300 ]
Term information
- DOID:0110874 (MONDO:equivalentTo)
- OMIM:605934 (MONDO:equivalentTo)
- UMLS:C1853830 (OMIM:605934)
- MESH:C565274 (MONDO:equivalentTo)
A holoprosencephaly that has material basis in variation in the chromosome region 2q37.1-q37.3.
http://identifiers.org/mesh/C565274
http://identifiers.org/omim/605934
http://linkedlifedata.com/resource/umls/id/C1853830
http://purl.obolibrary.org/obo/DOID_0110874