Phenotypic Abnormality (PA): Abnormality of lateral ventricle

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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:	Phenotypic abnormality [HP:0000118] <25>
+ + + + + 5:	Abnormality of the nervous system [HP:0000707] <4>	(142|168)	(156|103|45)
+ + + + 4:	Abnormality of nervous system morphology [HP:0012639] <5>	(69|97)	(79|52|16)
+ + + 3:	Morphological abnormality of the central nervous system [HP:0002011] <17>	(60|85)	(69|44|16)
+ + 2:	Abnormality of brain morphology [HP:0012443] <13>	(43|63)	(53|34|15)
+ 1:	Abnormality of the cerebral ventricles [HP:0002118] <11>	(3|6)	(6|1|3)
0:	Abnormality of lateral ventricle [HP:0030047] <2>	(0|2)	(2|1|0)
- 1:	Colpocephaly [HP:0030048]	(0|0)	(0|0|0)
- 1:	Dilation of lateral ventricles [HP:0006956]	(0|0)	(0|0|0)

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Family

Family domains annotated to this HP term (SDHP level: Highly Informative)
Highlighted in gray are those with FDR_all>0.001

SCOP term	FDR (all)	Annotation (direct or inherited)
Tubulin, GTPase domain	0.000867	DIRECT
Tubulin, C-terminal domain	0.000867	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)
Tubulin nucleotide-binding domain-like	0.0007523	DIRECT
Tubulin C-terminal domain-like	0.0007523	DIRECT

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

Supra-domain (Duplex) in N- to C-terminal order	FDR (all)	Annotation (direct or inherited)
52490,55307 52490 - Tubulin nucleotide-binding domain-like 55307 - Tubulin C-terminal domain-like	0.0007523	DIRECT