Human Phenotype Ontology

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Hello! Guest! Please Login or Register! Clinician Mode

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:
Deviation of the hand or of fingers of the hand (HP:0009484)

Parent Node:
Deviation of finger (HP:0004097)

Parent Node:
Ulnar deviation of the hand or of fingers of the hand (HP:0001193)

..Starting node
..Ulnar deviation of finger (HP:0009465)

Term ID:

9465

Name:

Ulnar deviation of finger

Synonym:

Finger bends toward pinky; Ulnar Drift

Definition:

Bending or curvature of a finger toward the ulnar side (i.e., away from the thumb). The deviation is at the metacarpal-phalangeal joint, and this finding is distinct from clinodactyly.

Comments:

Reference:

HP:0009465

Genes and Diseases:

Child Nodes:

........

Ulnar deviation of thumb (HP:0006156)

........

Ulnar deviation of the 5th finger (HP:0009180)

........

Ulnar deviation of the 4th finger (HP:0009278)

........

Ulnar deviation of the 3rd finger (HP:0009463)

........

Ulnar deviation of the 2nd finger (HP:0009464)

Sister Nodes:

Ulnar deviation of the hand (HP:0009487)

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:0009465	HP:0009465	Ulnar deviation of finger	0	ANKRD11 CL E G H	29123	21316	OMIM:148050	Kbg syndrome		102
HP:0009465	HP:0009465	Ulnar deviation of finger	0	B3GALT6 CL E G H	126792	17978	ORPHA:93359	Spondyloepimetaphyseal dysplasia with joint laxity	HP:0040283 - Occasional	38
HP:0009465	HP:0009465	Ulnar deviation of finger	0	BCR CL E G H	613	1014	ORPHA:261330	Distal 22q11.2 microdeletion syndrome	HP:0040283 - Occasional	5
HP:0009465	HP:0009465	Ulnar deviation of finger	0	BMP2 CL E G H	650	1069	OMIM:112600	Brachydactyly, type A2		13
HP:0009465	HP:0009465	Ulnar deviation of finger	0	BMPR1B CL E G H	658	1077	ORPHA:93384	Brachydactyly type C	HP:0040281 - Very frequent	90
HP:0009465	HP:0009465	Ulnar deviation of finger	0	BMPR1B CL E G H	658	1077	OMIM:112600	Brachydactyly, type A2		90
HP:0009465	HP:0009465	Ulnar deviation of finger	0	CD96 CL E G H	10225	16892	OMIM:211750	C syndrome	.	83
HP:0009465	HP:0009465	Ulnar deviation of finger	0	CHRNG CL E G H	1146	1967	OMIM:265000	Multiple pterygium syndrome, escobar variant		68
HP:0009465	HP:0009465	Ulnar deviation of finger	0	CRKL CL E G H	1399	2363	ORPHA:261330	Distal 22q11.2 microdeletion syndrome	HP:0040283 - Occasional
HP:0009465	HP:0009465	Ulnar deviation of finger	0	DACT1 CL E G H	51339	17748	ORPHA:857	Townes-Brocks syndrome	HP:0040283 - Occasional	2
HP:0009465	HP:0009465	Ulnar deviation of finger	0	DHCR7 CL E G H	1717	2860	ORPHA:818	Smith-Lemli-Opitz syndrome	HP:0040283 - Occasional	159
HP:0009465	HP:0009465	Ulnar deviation of finger	0	EXOC6B CL E G H	23233	17085	ORPHA:93359	Spondyloepimetaphyseal dysplasia with joint laxity	HP:0040283 - Occasional	3
HP:0009465	HP:0009465	Ulnar deviation of finger	0	FBN2 CL E G H	2201	3604	OMIM:121050	Contractural arachnodactyly, congenital	.	655
HP:0009465	HP:0009465	Ulnar deviation of finger	0	GDF5 CL E G H	8200	4220	ORPHA:93384	Brachydactyly type C	HP:0040281 - Very frequent	52
HP:0009465	HP:0009465	Ulnar deviation of finger	0	GDF5 CL E G H	8200	4220	OMIM:112600	Brachydactyly, type A2		52
HP:0009465	HP:0009465	Ulnar deviation of finger	0	GDF5 CL E G H	8200	4220	OMIM:113100	Brachydactyly, type C		52
HP:0009465	HP:0009465	Ulnar deviation of finger	0	HOXA13 CL E G H	3209	5102	OMIM:140000	Hand-Foot-Genital syndrome		11
HP:0009465	HP:0009465	Ulnar deviation of finger	0	HOXD13 CL E G H	3239	5136	ORPHA:93406	Syndactyly type 5	HP:0040281 - Very frequent	25
HP:0009465	HP:0009465	Ulnar deviation of finger	0	HRAS CL E G H	3265	5173	ORPHA:3071	Costello syndrome	HP:0040282 - Frequent	113
HP:0009465	HP:0009465	Ulnar deviation of finger	0	LIFR CL E G H	3977	6597	OMIM:601559	Stuve-Wiedemann syndrome	.	144
HP:0009465	HP:0009465	Ulnar deviation of finger	0	MAPK1 CL E G H	5594	6871	ORPHA:261330	Distal 22q11.2 microdeletion syndrome	HP:0040283 - Occasional	2
HP:0009465	HP:0009465	Ulnar deviation of finger	0	MYBPC1 CL E G H	4604	7549	ORPHA:1146	Distal arthrogryposis type 1	HP:0040282 - Frequent	66
HP:0009465	HP:0009465	Ulnar deviation of finger	0	MYH3 CL E G H	4621	7573	ORPHA:1146	Distal arthrogryposis type 1	HP:0040282 - Frequent	166
HP:0009465	HP:0009465	Ulnar deviation of finger	0	MYH3 CL E G H	4621	7573	ORPHA:2053	Freeman-Sheldon syndrome	HP:0040281 - Very frequent	166
HP:0009465	HP:0009465	Ulnar deviation of finger	0	MYH3 CL E G H	4621	7573	ORPHA:1147	Sheldon-Hall syndrome	HP:0040282 - Frequent	166
HP:0009465	HP:0009465	Ulnar deviation of finger	0	MYMK CL E G H	389827	33778	ORPHA:1358	Carey-Fineman-Ziter syndrome	HP:0040283 - Occasional	5
HP:0009465	HP:0009465	Ulnar deviation of finger	0	MYMX CL E G H	101929726	52391	ORPHA:1358	Carey-Fineman-Ziter syndrome	HP:0040283 - Occasional
HP:0009465	HP:0009465	Ulnar deviation of finger	0	NALCN CL E G H	259232	19082	ORPHA:1146	Distal arthrogryposis type 1	HP:0040282 - Frequent	48
HP:0009465	HP:0009465	Ulnar deviation of finger	0	NALCN CL E G H	259232	19082	ORPHA:2053	Freeman-Sheldon syndrome	HP:0040281 - Very frequent	48
HP:0009465	HP:0009465	Ulnar deviation of finger	0	NALCN CL E G H	259232	19082	ORPHA:1147	Sheldon-Hall syndrome	HP:0040282 - Frequent	48
HP:0009465	HP:0009465	Ulnar deviation of finger	0	PAX3 CL E G H	5077	8617	ORPHA:1529	Craniofacial-deafness-hand syndrome	HP:0040281 - Very frequent	59
HP:0009465	HP:0009465	Ulnar deviation of finger	0	PTRH2 CL E G H	51651	24265	ORPHA:456312	Infantile multisystem neurologic-endocrine-pancreatic disease		6
HP:0009465	HP:0009465	Ulnar deviation of finger	0	RAB3GAP1 CL E G H	22930	17063	ORPHA:1387	Cataract-intellectual disability-hypogonadism syndrome	HP:0040282 - Frequent	90
HP:0009465	HP:0009465	Ulnar deviation of finger	0	RAB3GAP2 CL E G H	25782	17168	ORPHA:1387	Cataract-intellectual disability-hypogonadism syndrome	HP:0040282 - Frequent	135
HP:0009465	HP:0009465	Ulnar deviation of finger	0	SALL1 CL E G H	6299	10524	ORPHA:857	Townes-Brocks syndrome	HP:0040283 - Occasional	124
HP:0009465	HP:0009465	Ulnar deviation of finger	0	SHOX CL E G H	6473	10853	ORPHA:2632	Langer mesomelic dysplasia	HP:0040281 - Very frequent	66
HP:0009465	HP:0009465	Ulnar deviation of finger	0	SLC26A2 CL E G H	1836	10994	ORPHA:628	Diastrophic dysplasia	HP:0040282 - Frequent	166
HP:0009465	HP:0009465	Ulnar deviation of finger	0	SLC26A2 CL E G H	1836	10994	OMIM:222600	Diastrophic dysplasia	.	166
HP:0009465	HP:0009465	Ulnar deviation of finger	0	TBX22 CL E G H	50945	11600	ORPHA:921	Abruzzo-Erickson syndrome	HP:0040282 - Frequent	28
HP:0009465	HP:0009465	Ulnar deviation of finger	0	TGDS CL E G H	23483	20324	OMIM:616145	Catel-Manzke syndrome		6
HP:0009465	HP:0009465	Ulnar deviation of finger	0	TNNI2 CL E G H	7136	11946	ORPHA:1146	Distal arthrogryposis type 1	HP:0040282 - Frequent	37
HP:0009465	HP:0009465	Ulnar deviation of finger	0	TNNI2 CL E G H	7136	11946	ORPHA:1147	Sheldon-Hall syndrome	HP:0040282 - Frequent	37
HP:0009465	HP:0009465	Ulnar deviation of finger	0	TNNT3 CL E G H	7140	11950	ORPHA:1146	Distal arthrogryposis type 1	HP:0040282 - Frequent	43
HP:0009465	HP:0009465	Ulnar deviation of finger	0	TNNT3 CL E G H	7140	11950	ORPHA:1147	Sheldon-Hall syndrome	HP:0040282 - Frequent	43
HP:0009465	HP:0009465	Ulnar deviation of finger	0	TPM2 CL E G H	7169	12011	ORPHA:1146	Distal arthrogryposis type 1	HP:0040282 - Frequent	54
HP:0009465	HP:0009465	Ulnar deviation of finger	0	TPM2 CL E G H	7169	12011	ORPHA:1147	Sheldon-Hall syndrome	HP:0040282 - Frequent	54
HP:0009465	HP:0009465	Ulnar deviation of finger	0	WNT7A CL E G H	7476	12786	OMIM:228930	Fibular aplasia or hypoplasia, femoral bowing and poly-, syn-, and oligodactyly		13
HP:0009465	HP:0006156	Ulnar deviation of thumb	1	CL E G H
HP:0009465	HP:0009278	Ulnar deviation of the 4th finger	1	CL E G H
HP:0009465	HP:0009180	Ulnar deviation of the 5th finger	1	CL E G H
HP:0009465	HP:0009464	Ulnar deviation of the 2nd finger	1	ANKRD11 CL E G H	29123	21316	OMIM:148050	Kbg syndrome		102
HP:0009465	HP:0009464	Ulnar deviation of the 2nd finger	1	BMP2 CL E G H	650	1069	OMIM:112600	Brachydactyly, type A2	.	13
HP:0009465	HP:0009464	Ulnar deviation of the 2nd finger	1	BMPR1B CL E G H	658	1077	OMIM:112600	Brachydactyly, type A2	.	90
HP:0009465	HP:0009464	Ulnar deviation of the 2nd finger	1	GDF5 CL E G H	8200	4220	OMIM:112600	Brachydactyly, type A2	.	52
HP:0009465	HP:0009464	Ulnar deviation of the 2nd finger	1	GDF5 CL E G H	8200	4220	OMIM:113100	Brachydactyly, type C	HP:0040282 - Frequent	52
HP:0009465	HP:0009463	Ulnar deviation of the 3rd finger	1	GDF5 CL E G H	8200	4220	OMIM:113100	Brachydactyly, type C	HP:0040282 - Frequent	52
HP:0009465	HP:0009464	Ulnar deviation of the 2nd finger	1	HOXA13 CL E G H	3209	5102	OMIM:140000	Hand-Foot-Genital syndrome	.	11
HP:0009465	HP:0009464	Ulnar deviation of the 2nd finger	1	PTRH2 CL E G H	51651	24265	ORPHA:456312	Infantile multisystem neurologic-endocrine-pancreatic disease	HP:0040283 - Occasional	6
HP:0009465	HP:0009463	Ulnar deviation of the 3rd finger	1	PTRH2 CL E G H	51651	24265	ORPHA:456312	Infantile multisystem neurologic-endocrine-pancreatic disease	HP:0040283 - Occasional	6
HP:0009465	HP:0009464	Ulnar deviation of the 2nd finger	1	TGDS CL E G H	23483	20324	OMIM:616145	Catel-Manzke syndrome	.	6

Genes (36) :ANKRD11 B3GALT6 BCR BMP2 BMPR1B CD96 CHRNG CRKL DACT1 DHCR7 EXOC6B FBN2 GDF5 HOXA13 HOXD13 HRAS LIFR MAPK1 MYBPC1 MYH3 MYMK MYMX NALCN PAX3 PTRH2 RAB3GAP1 RAB3GAP2 SALL1 SHOX SLC26A2 TBX22 TGDS TNNI2 TNNT3 TPM2 WNT7A

Diseases (28) :OMIM:148050 ORPHA:93359 ORPHA:261330 OMIM:112600 ORPHA:93384 OMIM:211750 OMIM:265000 ORPHA:857 ORPHA:818 OMIM:121050 OMIM:113100 OMIM:140000 ORPHA:93406 ORPHA:3071 OMIM:601559 ORPHA:1146 ORPHA:2053 ORPHA:1147 ORPHA:1358 ORPHA:1529 ORPHA:456312 ORPHA:1387 ORPHA:2632 ORPHA:628 OMIM:222600 ORPHA:921 OMIM:616145 OMIM:228930

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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