Phenotypic Abnormality (PA): Abnormal cardiomyocyte 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)
+ + + 3:	Phenotypic abnormality [HP:0000118] <25>
+ + + 3:	Abnormality of the cardiovascular system [HP:0001626] <5>	(60|88)	(73|43|30)
+ + 2:	Abnormal cellular phenotype [HP:0025354] <3>	(10|10)	(13|3|0)
+ + 2:	Abnormality of cardiovascular system morphology [HP:0030680] <3>	(29|42)	(31|19|20)
+ 1:	Abnormal heart morphology [HP:0001627] <16>	(20|35)	(24|16|20)
+ 1:	Abnormal cell morphology [HP:0025461] <7>	(0|0)	(0|0|0)
0:	Abnormal cardiomyocyte morphology [HP:0031331] <9>	(0|0)	(0|0|0)
- 1:	Abnormal cardiomyocyte mitochondrial morphology [HP:0031335] <1>	(0|0)	(0|0|0)
- 1:	Abnormal cadiomyocyte dystrophin staining [HP:0031339]	(0|0)	(0|0|0)
- 1:	Abnormal cardiomyocyte connexin43 staining [HP:0031337]	(0|0)	(0|0|0)
- 1:	Abnormal cardiomyocyte plakoglobin staining [HP:0031338]	(0|0)	(0|0|0)
- 1:	Cardiomyocyte degeneration [HP:0031332]	(0|0)	(0|0|0)
- 1:	Cardiomyocyte hypertrophy [HP:0031319]	(0|0)	(0|0|0)
- 1:	Cardiomyocyte inclusion bodies [HP:0031334]	(0|0)	(0|0|0)
- 1:	Cardiomyocyte mitochondrial proliferation [HP:0031320]	(0|0)	(0|0|0)
- 1:	Myocardial sarcomeric disarray [HP:0031333]	(0|0)	(0|0|0)

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