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Phenotypic Abnormality (PA): Neoplasm of the parathyroid gland

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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> #Domains
(Superfamily|Family)
#Supra-domain
(Single|Duplex|Triple)
+ + + 3:   Phenotypic abnormality [HP:0000118] <25>
+ + + 3:   Neoplasm [HP:0002664] <2>(20|21) (23|8|3)
+ + 2:   Abnormality of the endocrine system [HP:0000818] <16>(28|35) (35|13|5)
+ + 2:   Abnormality of the parathyroid gland [HP:0000828] <2>(0|0) (1|0|0)
+ + 2:   Neoplasm by anatomical site [HP:0011793] <24>(18|19) (20|7|2)
+ 1:   Neoplasm of the endocrine system [HP:0100568] <6>(6|5) (6|3|0)
+ 1:   Abnormality of the parathyroid morphology [HP:0011766] <3>(0|0) (0|0|0)
0:   Neoplasm of the parathyroid gland [HP:0100733] <2>(0|0) (0|0|0)
- 1:   Parathyroid adenoma [HP:0002897](0|0) (0|0|0)
- 1:   Parathyroid carcinoma [HP:0006780](0|0) (0|0|0)