Phenotypic Abnormality (PA): Thyroid adenoma

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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)
+ + + + 4:	Neoplasm [HP:0002664] <2>	(20|21)	(23|8|3)
+ + + + 4:	Phenotypic abnormality [HP:0000118] <25>
+ + + 3:	Abnormality of the endocrine system [HP:0000818] <16>	(28|35)	(35|13|5)
+ + + 3:	Neoplasm by anatomical site [HP:0011793] <24>	(18|19)	(20|7|2)
+ + + 3:	Abnormality of the thyroid gland [HP:0000820] <2>	(8|7)	(8|3|0)
+ + 2:	Neoplasm of the endocrine system [HP:0100568] <6>	(6|5)	(6|3|0)
+ + 2:	Abnormality of thyroid morphology [HP:0011772] <8>	(7|6)	(7|3|0)
+ 1:	Neoplasm of the thyroid gland [HP:0100031] <2>	(6|5)	(6|3|0)
0:	Thyroid adenoma [HP:0000854] <4>	(1|0)	(1|0|0)
- 1:	Thyroid follicular adenoma [HP:0011774] <2>	(0|0)	(0|0|0)
- 1:	Hurthle cell thyroid adenoma [HP:0006781]	(0|0)	(0|0|0)
- 1:	Thyroid atypical adenoma [HP:0011778]	(0|0)	(0|0|0)
- 1:	Thyroid papillary adenoma [HP:0011777]	(0|0)	(0|0|0)

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Superfamily

Superfamily domains annotated to this HP term (Not in SDHP)
Highlighted in gray are those with FDR_all>0.001

SCOP term	FDR (all)	Annotation (direct or inherited)
C2 domain (Calcium/lipid-binding domain, CaLB)	0.0002793	DIRECT

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Supra-domain (including individual superfamily)

Supra-domains annotated to this HP term (Not in SPHO)
Highlighted in gray are those with FDR>0.001

Supra-domain (Single)	FDR (all)	Annotation (direct or inherited)
C2 domain (Calcium/lipid-binding domain, CaLB)	0.0001368	DIRECT