Human Phenotype Ontology 
Grandparent Node:
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Abnormality of finger (HP:0001167)help
Grandparent Node:
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Deviation of the hand or of fingers of the hand (HP:0009484)help
Parent Node:
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Abnormal 4th finger morphology (HP:0004188)help
Parent Node:
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Deviation of finger (HP:0004097)help
..Starting node
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Deviation of the 4th finger (HP:0009273)help
Term ID: 9273
Name: Deviation of the 4th finger
Synonym: Deviation of the ring finger
Definition: Displacement of the 4th finger from its normal position.
Comments:
Reference: HP:0009273
Genes and Diseases:
 
       Child Nodes:
........expandUlnar deviation of the 4th finger (HP:0009278) help
........expandRadial deviation of the 4th finger (HP:0009279) help
........expandClinodactyly of the 4th finger (HP:0040025) help

 Sister Nodes: 
..expandDeviation of the 2nd finger (HP:0009468) help
..expandDeviation of the 3rd finger (HP:0009317) help
..expandDeviation of the 5th finger (HP:0009179) help
..expandDeviation of the thumb (HP:0009603) help
..expandFinger clinodactyly (HP:0040019) help
..expandOverlapping fingers (HP:0010557) help
..expandRadial deviation of finger (HP:0009466) help
..expandUlnar deviation of finger (HP:0009465) help
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0009273HP:0009273Deviation of the 4th finger0ABCC8 CL E G H683359ORPHA:79134DEND syndrome245
HP:0009273HP:0009273Deviation of the 4th finger0COL11A1 CL E G H13012186OMIM:154780Marshall syndrome215
HP:0009273HP:0009273Deviation of the 4th finger0IHH CL E G H35495956OMIM:112500Brachydactyly, type A144
HP:0009273HP:0009273Deviation of the 4th finger0KCNJ11 CL E G H37676257ORPHA:79134DEND syndrome127
HP:0009273HP:0009273Deviation of the 4th finger0KNSTRN CL E G H9041730767ORPHA:221139Combined immunodeficiency with faciooculoskeletal anomalies1
HP:0009273HP:0009273Deviation of the 4th finger0NARS2 CL E G H7973126274ORPHA:79134DEND syndrome34
HP:0009273HP:0009273Deviation of the 4th finger0PIK3CD CL E G H52938977ORPHA:221139Combined immunodeficiency with faciooculoskeletal anomalies9
HP:0009273HP:0009273Deviation of the 4th finger0SNRPN CL E G H663811164ORPHA:177907Prader-Willi syndrome due to translocation37
HP:0009273HP:0009278Ulnar deviation of the 4th finger1 CL E G H
HP:0009273HP:0040025Clinodactyly of the 4th finger1ABCC8 CL E G H683359ORPHA:79134DEND syndromeHP:0040283 - Occasional245
HP:0009273HP:0040025Clinodactyly of the 4th finger1COL11A1 CL E G H13012186OMIM:154780Marshall syndrome215
HP:0009273HP:0009279Radial deviation of the 4th finger1IHH CL E G H35495956OMIM:112500Brachydactyly, type A1.44
HP:0009273HP:0040025Clinodactyly of the 4th finger1KCNJ11 CL E G H37676257ORPHA:79134DEND syndromeHP:0040283 - Occasional127
HP:0009273HP:0040025Clinodactyly of the 4th finger1KNSTRN CL E G H9041730767ORPHA:221139Combined immunodeficiency with faciooculoskeletal anomaliesHP:0040282 - Frequent1
HP:0009273HP:0040025Clinodactyly of the 4th finger1NARS2 CL E G H7973126274ORPHA:79134DEND syndromeHP:0040283 - Occasional34
HP:0009273HP:0040025Clinodactyly of the 4th finger1PIK3CD CL E G H52938977ORPHA:221139Combined immunodeficiency with faciooculoskeletal anomaliesHP:0040282 - Frequent9
HP:0009273HP:0040025Clinodactyly of the 4th finger1SNRPN CL E G H663811164ORPHA:177907Prader-Willi syndrome due to translocationHP:0040283 - Occasional37


Genes (8) :ABCC8 COL11A1 IHH KCNJ11 KNSTRN NARS2 PIK3CD SNRPN

Diseases (5) :ORPHA:79134 OMIM:154780 OMIM:112500 ORPHA:221139 ORPHA:177907
 

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