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 5th finger phalanx morphology (HP:0004213)

Grandparent Node:
Curved fingers (HP:0004095)

Grandparent Node:
Curved phalanges of the hand (HP:0009770)

Parent Node:
Abnormality of the middle phalanx of the 5th finger (HP:0004219)

Parent Node:
Curved middle phalanges of the hand (HP:0009846)

Parent Node:
Curved phalanges of the 5th finger (HP:0004214)

..Starting node
..Curved middle phalanx of the 5th finger (HP:0009173)

Term ID:

9173

Name:

Curved middle phalanx of the 5th finger

Synonym:

Curved middle bone of little finger; Curved middle bone of pinkie finger; Curved middle bone of pinky finger

Definition:

Curved appearance of the middle phalanx of the 5th finger.

Comments:

Reference:

HP:0009173

Genes and Diseases:

Child Nodes:

Sister Nodes:

Curved distal phalanx of the 5th finger (HP:0004226)

Curved proximal phalanx of the 5th finger (HP:0009229)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0009173	HP:0009173	Curved middle phalanx of the 5th 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.