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:
Sclerosis of 3rd finger phalanx (HP:0100919)

Grandparent Node:
Sclerosis of middle finger phalanx (HP:0100916)

Parent Node:
Abnormality of the middle phalanx of the 3rd finger (HP:0004172)

Parent Node:
Patchy sclerosis of 3rd finger phalanx (HP:0009444)

Parent Node:
Patchy sclerosis of middle phalanx of finger (HP:0009848)

Parent Node:
Sclerosis of the middle phalanx of the 3rd finger (HP:0100905)

..Starting node
..Patchy sclerosis of the middle phalanx of the 3rd finger (HP:0009434)

Term ID:

9434

Name:

Patchy sclerosis of the middle phalanx of the 3rd finger

Synonym:

Uneven increase in bone density in the middle bone of the middle finger

Definition:

Uneven (irregular) increase in bone density of the middle phalanx of the third finger.

Comments:

Reference:

HP:0009434

Genes and Diseases:

Child Nodes:

Sister Nodes:

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0009434	HP:0009434	Patchy sclerosis of the middle phalanx of the 3rd finger	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.