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Phenotypic Abnormality (PA): Hamartoma

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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)
+ + + 3:   Phenotypic abnormality [HP:0000118] <25>
+ + 2:   Neoplasm [HP:0002664] <2>(20|21) (23|8|3)
+ 1:   Neoplasm by histology [HP:0011792] <7>(5|7) (6|3|0)
0:   Hamartoma [HP:0010566] <10>(0|0) (0|0|0)
- 1:   Cerebral hamartoma [HP:0009731] <3>(0|0) (0|0|0)
- 1:   Hamartoma of the eye [HP:0010568] <3>(0|0) (0|0|0)
- 1:   Hamartomatous polyposis [HP:0004390] <3>(0|0) (0|0|0)
- 1:   Lymphangioma [HP:0100764] <2>(0|0) (0|0|0)
- 1:   Renal hamartoma [HP:0008696] <1>(0|0) (0|0|0)
- 1:   Chorangioma [HP:0100883](0|0) (0|0|0)
- 1:   Cutaneous hamartoma [HP:0031111](0|0) (0|0|0)
- 1:   Fibrous hamartoma [HP:0100882](0|0) (0|0|0)
- 1:   Numerous nevi [HP:0001054](0|0) (0|0|0)
- 1:   Odontoma [HP:0011068](0|0) (0|0|0)