bn:17554325n
Noun Concept
Categories: Syndromes with microcephaly, Syndromes with cleft lip and/or palate, Syndromes affecting the jaw, Syndromes affecting teeth, Syndromes with craniofacial abnormalities
EN
13q deletion syndrome
EN
13q deletion syndrome is a rare genetic disease caused by the deletion of some or all of the large arm of human chromosome 13. Wikipedia
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EN
13q deletion syndrome is a rare genetic disease caused by the deletion of some or all of the large arm of human chromosome 13. Wikipedia
medical condition Wikidata
Wikipedia
Wikidata