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Q38045752-07EB5F9B-1802-42D3-A4F3-F4B144E80060
Q38045752-07EB5F9B-1802-42D3-A4F3-F4B144E80060
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Statement
http://www.wikidata.org/entity/statement/Q38045752-07EB5F9B-1802-42D3-A4F3-F4B144E80060
Chromosomal and related Mendelian syndromes associated with Hirschsprung's disease.
P2860
Q38045752-07EB5F9B-1802-42D3-A4F3-F4B144E80060
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38045752-07EB5F9B-1802-42D3-A4F3-F4B144E80060
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wasDerivedFrom
68860a55c3b8eb5d04e1077fb0bd10fdc4fd6dae
P2860
A case of Hirschsprung disease with a chromosome 13 microdeletion, del(13)(q32.3q33.2): potential mapping of one disease locus.