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:
Abnormal palm morphology (HP:0100871)

Grandparent Node:
Regional abnormality of skin (HP:0011356)

Parent Node:
Abnormal skin morphology of the palm (HP:0040211)

..Starting node
..Palmar edema (HP:0025538)

Term ID:

25538

Name:

Palmar edema

Synonym:

Palmar oedema

Definition:

An abnormal accumulation of fluid beneath the skin on the palm of the hand.

Comments:

Reference:

HP:0025538

Genes and Diseases:

Child Nodes:

Sister Nodes:

Abnormal palmar dermatoglyphics (HP:0001018)

Excessive wrinkling of palmar skin (HP:0007605)

Palmar hyperhidrosis (HP:0006089)

Palmar hyperkeratosis (HP:0010765)

Palmar pits (HP:0010610)

Palmar telangiectasia (HP:0100869)

Palmoplantar blistering (HP:0007446)

Palmoplantar cutis gyrata (HP:0007469)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0025538	HP:0025538	Palmar edema	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.