Distal trisomy 7p is a rare chromosomal anomaly syndrome, resulting from the partial duplication of the short arm of chromosome 7, with highly variable phenotype typically characterized by severe to profound psychomotor delay, intellectual disability, dysmorphic features (incl. dolichocephaly, microbrachycephaly, high and/or broad forehead, large anterior fontanel, hypertelorism, downslanting palpebral fissures, low-set, dysplastic ears, low, broad and prominent nasal bridge, abnormal palate, micro-/retrognathia), and hypotonia. Cardiovascular, gastrointestinal, skeletal and urogenital anomalies have commonly been reported. [ Orphanet:96074 ]
Synonyms: trisomy 7pter distal duplication 7p telomeric duplication 7p distal trisomy type 7p
Term information
- SCTID:763276000 (MONDO:equivalentTo)
- UMLS:C4706364 (MONDO:equivalentTo)
- GARD:19307 (MONDO:GARD)
- Orphanet:96074 (MONDO:equivalentTo)
- MEDGEN:1641655 (MONDO:equivalentTo)
gard_rare, ordo_disorder, rare, ordo_malformation_syndrome, nord_rare, orphanet_rare
http://www.orpha.net/ORDO/Orphanet_96074
http://identifiers.org/medgen/1641655
http://identifiers.org/snomedct/763276000
http://linkedlifedata.com/resource/umls/id/C4706364