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:
Finger symphalangism (HP:0009700)

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

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

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

Parent Node:
Symphalangism of the 5th finger (HP:0004218)

..Starting node
..Symphalangism of middle phalanx of 5th finger (HP:0009178)

Term ID:

9178

Name:

Symphalangism of middle phalanx of 5th finger

Synonym:

Fused middle bones of little finger; Fused middle bones of pinkie finger; Fused middle bones of pinky finger

Definition:

Fusion of the middle phalanx of the 5th finger with another bone.

Comments:

Reference:

HP:0009178

Genes and Diseases:

Child Nodes:

........

Proximal/middle symphalangism of 5th finger (HP:0009177)

........

Distal/middle symphalangism of 5th finger (HP:0009244)

Sister Nodes:

Symphalangism affecting the proximal phalanx of the 5th finger (HP:0009232)

Input	HPO ID	HPO term	Distance	Gene	Gene id entrez	HGNC ID	DiseaseId	DiseaseName	Frequency	ClinVar variants
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0009178	HP:0009178	Symphalangism of middle phalanx of 5th finger	0	BHLHA9 CL E G H	727857	35126	OMIM:609432	Syndactyly, mesoaxial synostotic, with phalangeal reduction		4
HP:0009178	HP:0009178	Symphalangism of middle phalanx of 5th finger	0	GDF5 CL E G H	8200	4220	OMIM:615298	SYMPHALANGISM, PROXIMAL, 1B; SYM1B		52
HP:0009178	HP:0009178	Symphalangism of middle phalanx of 5th finger	0	NOG CL E G H	9241	7866	OMIM:186500	Multiple synostoses syndrome 1		22
HP:0009178	HP:0009178	Symphalangism of middle phalanx of 5th finger	0	NOG CL E G H	9241	7866	OMIM:184460	Stapes ankylosis with broad thumb and toes		22
HP:0009178	HP:0009178	Symphalangism of middle phalanx of 5th finger	0	ROR2 CL E G H	4920	10257	OMIM:268310	Robinow syndrome, autosomal recessive		120
HP:0009178	HP:0009178	Symphalangism of middle phalanx of 5th finger	0	TFAP2B CL E G H	7021	11743	OMIM:169100	Char syndrome		104
HP:0009178	HP:0009177	Proximal/middle symphalangism of 5th finger	1	BHLHA9 CL E G H	727857	35126	OMIM:609432	Syndactyly, mesoaxial synostotic, with phalangeal reduction	.	4
HP:0009178	HP:0009177	Proximal/middle symphalangism of 5th finger	1	GDF5 CL E G H	8200	4220	OMIM:615298	SYMPHALANGISM, PROXIMAL, 1B; SYM1B		52
HP:0009178	HP:0009177	Proximal/middle symphalangism of 5th finger	1	NOG CL E G H	9241	7866	OMIM:186500	Multiple synostoses syndrome 1		22
HP:0009178	HP:0009177	Proximal/middle symphalangism of 5th finger	1	NOG CL E G H	9241	7866	OMIM:184460	Stapes ankylosis with broad thumb and toes	.	22
HP:0009178	HP:0009177	Proximal/middle symphalangism of 5th finger	1	ROR2 CL E G H	4920	10257	OMIM:268310	Robinow syndrome, autosomal recessive		120
HP:0009178	HP:0009244	Distal/middle symphalangism of 5th finger	1	TFAP2B CL E G H	7021	11743	OMIM:169100	Char syndrome	.	104

Genes (5) :BHLHA9 GDF5 NOG ROR2 TFAP2B

Diseases (6) :OMIM:609432 OMIM:615298 OMIM:186500 OMIM:184460 OMIM:268310 OMIM:169100

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

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