Phenotypic Abnormality (PA): Pinealoma

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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)
+ + + + + + 6:	Abnormality of the nervous system [HP:0000707] <4>	(142|168)	(156|103|45)
+ + + + + + 6:	Phenotypic abnormality [HP:0000118] <25>
+ + + + + 5:	Neoplasm by anatomical site [HP:0011793] <24>	(18|19)	(20|7|2)
+ + + + + 5:	Neoplasm [HP:0002664] <2>	(20|21)	(23|8|3)
+ + + + + 5:	Abnormality of nervous system morphology [HP:0012639] <5>	(69|97)	(79|52|16)
+ + + + 4:	Morphological abnormality of the central nervous system [HP:0002011] <17>	(60|85)	(69|44|16)
+ + + + 4:	Neoplasm of the nervous system [HP:0004375] <2>	(3|6)	(3|2|0)
+ + + + 4:	Neoplasm by histology [HP:0011792] <7>	(5|7)	(6|3|0)
+ + + 3:	Neoplasm of the central nervous system [HP:0100006] <5>	(3|6)	(3|2|0)
+ + + 3:	Nervous tissue neoplasm [HP:0030060] <1>	(3|6)	(3|2|0)
+ + 2:	Neuroectodermal neoplasm [HP:0030061] <2>	(3|6)	(3|2|0)
+ + 2:	Brain neoplasm [HP:0030692] <1>	(0|0)	(0|0|0)
+ 1:	Supratentorial neoplasm [HP:0030693] <1>	(0|0)	(0|0|0)
+ 1:	Neuroepithelial neoplasm [HP:0030063] <5>	(3|6)	(3|2|0)
0:	Pinealoma [HP:0010799] <1>	(0|0)	(0|0|0)
- 1:	Pineal parenchymal cell neoplasm [HP:0030694] <2>	(0|0)	(0|0|0)

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