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:
Morphological abnormality of the pyramidal tract (HP:0002062)

Parent Node:
Morphological abnormality of the corticospinal tract (HP:0002492)

..Starting node
..Corticospinal tract pallor (HP:0008361)

Term ID:

8361

Name:

Corticospinal tract pallor

Synonym:

Definition:

Comments:

Reference:

HP:0008361

Genes and Diseases:

Child Nodes:

Sister Nodes:

Aplasia/Hypoplasia involving the corticospinal tracts (HP:0007365)

Atrophy/Degeneration involving the corticospinal tracts (HP:0007372)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0008361	HP:0008361	Corticospinal tract pallor	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.