Phenotypic Abnormality (PA): Abnormality of neuronal migration

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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:	Phenotypic abnormality [HP:0000118] <25>
+ + + 3:	Abnormality of the nervous system [HP:0000707] <4>	(142|168)	(156|103|45)
+ + 2:	Abnormality of nervous system morphology [HP:0012639] <5>	(69|97)	(79|52|16)
+ 1:	Morphological abnormality of the central nervous system [HP:0002011] <17>	(60|85)	(69|44|16)
0:	Abnormality of neuronal migration [HP:0002269] <3>	(4|3)	(4|1|0)
- 1:	Abnormal cortical gyration [HP:0002536] <4>	(4|3)	(4|1|0)
- 1:	Dysgyria [HP:0032398] <2>	(0|0)	(0|0|0)
- 1:	Gray matter heterotopia [HP:0002282] <2>	(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)
Tubulin C-terminal domain-like	0.00005618	DIRECT
Tubulin nucleotide-binding domain-like	0.0001648	DIRECT
Adenine nucleotide alpha hydrolases-like	0.001169	INHERITED FROM: Abnormal cortical gyration
Nucleotide-diphospho-sugar transferases	0.2698	INHERITED FROM: Type II lissencephaly || Macrogyria

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Family

Family 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)
Tubulin, C-terminal domain	0.00002071	DIRECT
Tubulin, GTPase domain	0.00006778	DIRECT
Phoshoinositide 3-kinase (PI3K), catalytic domain	0.00009874	DIRECT

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Supra-domain (including individual superfamily)

Supra-domains annotated to this HP term (SPHO level: Highly Informative)
Highlighted in gray are those with FDR>0.001

Supra-domain (Single)	FDR (all)	Annotation (direct or inherited)
Tubulin C-terminal domain-like	0.00002528	DIRECT
Tubulin nucleotide-binding domain-like	0.0000778	DIRECT
Adenine nucleotide alpha hydrolases-like	0.000625	DIRECT
Nucleotide-diphospho-sugar transferases	0.2317	INHERITED FROM: Type II lissencephaly || Macrogyria

Supra-domains annotated to this HP term (SPHO level: Highly Informative)
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	0.00002528	DIRECT