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 palmar dermatoglyphics (HP:0001018)

Parent Node:
Abnormality of the palmar creases (HP:0010490)

..Starting node
..Prominent palmar flexion creases (HP:0006157)

Term ID:

6157

Name:

Prominent palmar flexion creases

Synonym:

Prominent life line

Definition:

Comments:

Reference:

HP:0006157

Genes and Diseases:

Child Nodes:

Sister Nodes:

Aplasia/Hypoplasia of the palmar creases (HP:0010488)

Bridged palmar crease (HP:0011310)

Deep palmar crease (HP:0006191)

Multiple palmar creases (HP:0006114)

Single transverse palmar crease (HP:0000954)

Sydney crease (HP:0011311)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0006157	HP:0006157	Prominent palmar flexion creases	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.