Synonyms: MEND syndrome, X-linked recessive MEND syndrome Male EBP disorder with neurological defects
This is just here as a test because I lose it
Term information
database
cross reference
- UMLS:C4085243 (MONDO:ncbi_mim2gene_medline)
- Orphanet:401973 (OMIM:300960)
- OMIM:300960 (Orphanet:401973/e)
- GARD:17666 (Orphanet:401973)
- DOID:0111865 (MONDO:equivalentTo)
Subsets
gard_rare, rare, ordo_malformation_syndrome, nord_rare, orphanet_rare, clingen
IAO 0000233
https://github.com/monarch-initiative/mondo/issues/5588
https://github.com/monarch-initiative/mondo/issues/4521
exactMatch
https://omim.org/entry/300960
http://www.orpha.net/ORDO/Orphanet_401973
http://linkedlifedata.com/resource/umls/id/C4085243
http://purl.obolibrary.org/obo/DOID_0111865