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 4th finger phalanx morphology (HP:0009172)

Grandparent Node:
Finger symphalangism (HP:0009700)

Grandparent Node:
Symphalangism affecting the phalanges of the hand (HP:0009773)

Parent Node:
Abnormality of the middle phalanx of the 4th finger (HP:0009283)

Parent Node:
Symphalangism of middle phalanx of finger (HP:0009849)

Parent Node:
Symphalangism of the 4th finger (HP:0004197)

..Starting node
..Symphalangism of middle phalanx of 4th finger (HP:0009308)

Term ID:

9308

Name:

Symphalangism of middle phalanx of 4th finger

Synonym:

Fused middle bone of ring finger

Definition:

Fusion of the middle phalanx of the 4th finger with another bone.

Comments:

Reference:

HP:0009308

Genes and Diseases:

Child Nodes:

........

Distal/middle symphalangism of 4th finger (HP:0009305)

........

Proximal/middle symphalangism of 4th finger (HP:0009477)

Sister Nodes:

Symphalangism affecting the proximal phalanx of the 4th finger (HP:0009314)

Input	HPO ID	HPO term	Distance	Gene	Gene id entrez	HGNC ID	DiseaseId	DiseaseName	ClinVar variants
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0009308	HP:0009308	Symphalangism of middle phalanx of 4th finger	0	NOG CL E G H	9241	7866	OMIM:186500	Multiple synostoses syndrome 1	22
HP:0009308	HP:0009305	Distal/middle symphalangism of 4th finger	1	CL E G H
HP:0009308	HP:0009477	Proximal/middle symphalangism of 4th finger	1	NOG CL E G H	9241	7866	OMIM:186500	Multiple synostoses syndrome 1	22

Genes (1) :NOG

Diseases (1) :OMIM:186500

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.