Human Phenotype Ontology

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Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

Grandparent Node:
Arteriosclerosis (HP:0002634)

Parent Node:
Atherosclerosis (HP:0002621)

..Starting node
..Fatty streak (HP:0031011)

Term ID:

31011

Name:

Fatty streak

Synonym:

Sudanophilic lesion

Definition:

Yellow-colored streaks, patches, or spots on the intimal surface of arteries. Fatty streaks stain red with Sudan III or Sudan IV.

Comments:

Reference:

HP:0031011

Genes and Diseases:

Child Nodes:

Sister Nodes:

Accelerated atherosclerosis (HP:0004943)

Aortic atherosclerotic lesion (HP:0012397)

Atherosclerotic lesion (HP:0031678)

Cerebral artery atherosclerosis (HP:0007201)

Coronary artery atherosclerosis (HP:0001677)

Foam cells (HP:0003651)

Precocious atherosclerosis (HP:0004416)

Thin-cap fibroatheroma (HP:0031012)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0031011	HP:0031011	Fatty streak	0	CL E G H

Genes (0) :

Diseases (0) :

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.