Preferred Label : Chromosome 21, uniparental disomy of;
UMLS semantic type : T049 - Cell or Molecular Dysfunction;
Origin ID : M0531255;
UMLS CUI : C2931324;
Currated CISMeF NLP mapping
- Related record
- Semantic type(s)
- UMLS correspondences (same concept)
http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=FR&Expert=96195
2011
France
scientific and technical information
chromosome 21, uniparental disomy of
uniparental disomy
chromosomes, human, pair 21
patulin
Chromosome 21, uniparental disomy of
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http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=FR&Expert=96187
2011
France
scientific and technical information
chromosomes, human, pair 21
purpura, thrombotic thrombocytopenic
chromosome 21, uniparental disomy of
uniparental disomy
Chromosome 21, uniparental disomy of
---
