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 epiphysis morphology of the phalanges of the hand (HP:0005920)

Grandparent Node:
Small epiphyses (HP:0010585)

Parent Node:
Abnormality of the epiphyses of the 5th finger (HP:0009152)

Parent Node:
Small epiphyses of the phalanges of the hand (HP:0010236)

..Starting node
..Small epiphyses of the 5th finger (HP:0009390)

Term ID:

9390

Name:

Small epiphyses of the 5th finger

Synonym:

Small end part of little finger bone; Small end part of pinkie finger bone; Small end part of pinky finger bone

Definition:

Abnormally small size of the epiphyses of the 5th finger with respect to age-dependent norms.

Comments:

Reference:

HP:0009390

Genes and Diseases:

Child Nodes:

........

Small epiphysis of the distal phalanx of the 5th finger (HP:0009148)

........

Small epiphysis of the proximal phalanx of the 5th finger (HP:0009159)

........

Small epiphysis of the middle phalanx of the 5th finger (HP:0009211)

Sister Nodes:

Small epiphyses of the 2nd finger (HP:0009496)

Small epiphyses of the 3rd finger (HP:0009418)

Small epiphyses of the 4th finger (HP:0009401)

Small epiphyses of the distal phalanges of the hand (HP:0010254)

Small epiphyses of the middle phalanges of the hand (HP:0010265)

Small epiphyses of the proximal phalanges of the hand (HP:0010276)

Small thumb epiphysis (HP:0009694)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0009390	HP:0009390	Small epiphyses of the 5th finger	0	CL E G H
HP:0009390	HP:0009211	Small epiphysis of the middle phalanx of the 5th finger	1	CL E G H
HP:0009390	HP:0009159	Small epiphysis of the proximal phalanx of the 5th finger	1	CL E G H
HP:0009390	HP:0009148	Small epiphysis of the distal phalanx of the 5th 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.