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3q26 microduplication syndrome

Go to external page http://purl.obolibrary.org/obo/MONDO_0019878

3q26 microduplication syndrome is a rare chromosomal anomaly characterized by prenatal and postnatal growth retardation, developmental delay, intellectual impairment, dysmorphic signs and variable combination of congenital anomalies, including cardiovascular, genitourinary and skeletal anomalies and spectrum of caudal malformations. [ Orphanet:96095 ]

Synonyms: Cornelia de Lange-like syndrome trisomy 3q26 dup(3)(q26) dup(3q) syndrome

This is just here as a test because I lose it

Term information

database cross reference
  • Orphanet:96095 (MONDO:equivalentTo)
  • GARD:19311 (MONDO:GARD)
  • MEDGEN:1670584 (MONDO:equivalentTo)
  • UMLS:C4755319 (MONDO:equivalentTo)
Subsets

ordo_disorder, gard_rare, otar, rare, ordo_malformation_syndrome, nord_rare, orphanet_rare

IAO 0000233

https://github.com/monarch-initiative/mondo/issues/3492

exactMatch

http://www.orpha.net/ORDO/Orphanet_96095

http://linkedlifedata.com/resource/umls/id/C4755319

http://identifiers.org/medgen/1670584

excluded subClassOf

http://purl.obolibrary.org/obo/MONDO_0020226

id

MONDO:0019878