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Mode of Inheritance (MI): Mode of inheritance

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Root: HP Hierarchy (human phenotype with 3 sub-ontologies PA, MI, ON)

Shortest distance to current term (+ for parents, - for children) HP term [HP ID] <#Children> (#SF|#FA) #Supra-domain
(Single|Duplex|Triple)
0:   Mode of inheritance [HP:0000005] <12>
- 1:   Autosomal dominant inheritance [HP:0000006] <6>(26|31) (26|26|15)
- 1:   Multifactorial inheritance [HP:0001426] <3>(1|2) (1|1|0)
- 1:   Gonosomal inheritance [HP:0010985] <2>(2|1) (2|1|0)
- 1:   Uniparental disomy [HP:0032382] <2>(0|0) (0|0|0)
- 1:   Autosomal recessive inheritance [HP:0000007] <1>(61|64) (61|39|18)
- 1:   Contiguous gene syndrome [HP:0001466] <1>(0|0) (0|0|0)
- 1:   Genetic anticipation [HP:0003743] <1>(0|0) (0|0|0)
- 1:   Somatic mutation [HP:0001428] <1>(5|6) (5|0|1)
- 1:   Heterogeneous [HP:0001425](4|4) (4|1|0)
- 1:   Mitochondrial inheritance [HP:0001427](0|0) (0|0|0)
- 1:   Semidominant mode of inheritance [HP:0032113](0|0) (0|0|0)
- 1:   Sporadic [HP:0003745](0|1) (0|0|1)