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 middle phalanx morphology of the hand (HP:0009833)

Grandparent Node:
Sclerosis of finger phalanx (HP:0100899)

Parent Node:
Sclerosis of 2nd finger phalanx (HP:0100918)

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

..Starting node
..Sclerosis of the middle phalanx of the 2nd finger (HP:0100904)

Term ID:

100904

Name:

Sclerosis of the middle phalanx of the 2nd finger

Synonym:

Increased bone density in the middle bone of the index finger

Definition:

Comments:

Reference:

HP:0100904

Genes and Diseases:

Child Nodes:

........

Patchy sclerosis of the middle phalanx of the 2nd finger (HP:0009573)

Sister Nodes:

Ivory epiphyses of the middle phalanges of the hand (HP:0010263)

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

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

Sclerosis of the middle phalanx of the 4th finger (HP:0100906)

Sclerosis of the middle phalanx of the 5th finger (HP:0100907)

Sclerosis of the proximal phalanx of the thumb (HP:0100913)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0100904	HP:0100904	Sclerosis of the middle phalanx of the 2nd finger	0	CL E G H
HP:0100904	HP:0009573	Patchy sclerosis of the middle phalanx of the 2nd finger	1	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.