Human Phenotype Ontology 
Grandparent Node:
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Abnormality of the hand (HP:0001155)help
Grandparent Node:
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Duplication of bones involving the upper extremities (HP:0009142)help
Parent Node:
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Abnormal carpal morphology (HP:0001191)help
Parent Node:
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Duplication of hand bones (HP:0004275)help
..Starting node
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Accessory carpal bones (HP:0004232)help
Term ID: 4232
Name: Accessory carpal bones
Synonym: Extra wrist bones; Supernumerary carpal bones
Definition: The presence of more than the normal number of carpal bones.
Comments:
Reference: HP:0004232
Genes and Diseases:
 
       Child Nodes:
........expandAccessory scaphoid (HP:0004244) help
........expandAccessory lunate (HP:0004249) help

 Sister Nodes: 
..expandDuplication of phalanx of hand (HP:0009997) 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:0004232HP:0004232Accessory carpal bones0FLNA CL E G H23163754OMIM:311300Otopalatodigital syndrome, type I.493
HP:0004232HP:0004232Accessory carpal bones0FLNB CL E G H23173755OMIM:150250Larsen syndrome.233
HP:0004232HP:0004232Accessory carpal bones0FLNB CL E G H23173755ORPHA:503Larsen syndromeHP:0040282 - Frequent233
HP:0004232HP:0004249Accessory lunate1 CL E G H
HP:0004232HP:0004244Accessory scaphoid1 CL E G H


Genes (2) :FLNA FLNB

Diseases (3) :OMIM:311300 OMIM:150250 ORPHA:503
 

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