SUPERFAMILY 1.75 HMM library and genome assignments server

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] <11>
- 1:   Autosomal dominant inheritance [HP:0000006] <5>(14|16) (14|11|6)
- 1:   Multifactorial inheritance [HP:0001426] <3>(1|0) (1|0|0)
- 1:   Gonosomal inheritance [HP:0010985] <2>(2|1) (3|0|0)
- 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>(1|1) (1|0|0)
- 1:   Autosomal recessive inheritance [HP:0000007](41|39) (42|27|10)
- 1:   Familial predisposition [HP:0001472](0|0) (0|0|0)
- 1:   Heterogeneous [HP:0001425](1|1) (1|0|0)
- 1:   Mitochondrial inheritance [HP:0001427](0|0) (0|0|0)
- 1:   Sporadic [HP:0003745](0|0) (0|0|0)