Phenotypic Abnormality (PA): Abnormal meningeal morphology

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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:	Abnormal meningeal morphology [HP:0010651] <7>	(0|0)	(0|1|1)
- 1:	Abnormal spinal meningeal morphology [HP:0010303] <6>	(0|0)	(0|0|0)
- 1:	Meningocele [HP:0002435] <6>	(0|0)	(0|0|0)
- 1:	Abnormal dura mater morphology [HP:0010652] <2>	(0|0)	(0|0|0)
- 1:	Abnormal arachnoid mater morphology [HP:0100700] <1>	(0|0)	(0|0|0)
- 1:	Abnormal pia mater [HP:0100701]	(0|0)	(0|0|0)
- 1:	Leptomeningeal enhancement [HP:0032070]	(0|0)	(0|0|0)
- 1:	Meningeal calcification [HP:0100250]	(0|0)	(0|0|0)

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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 (Duplex) in N- to C-terminal order	FDR (all)	Annotation (direct or inherited)
57196,57184 57196 - EGF/Laminin 57184 - Growth factor receptor domain	0.0009141	DIRECT

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

Supra-domain (Triple) in N- to C-terminal order	FDR (all)	Annotation (direct or inherited)
57196,57196,57184 57196 - EGF/Laminin 57196 - EGF/Laminin 57184 - Growth factor receptor domain	0.0009141	DIRECT

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