Human Phenotype Ontology 
Grandparent Node:
expandAbnormality of the upper limb (HP:0002817)help
Parent Node:
expandAbnormal arm span (HP:0012769)help
..Starting node
..expandIncreased arm span (HP:0012771)help
Term ID: 12771
Name: Increased arm span
Synonym: Increased arm span
Definition: Increased length of the arm span (length from one end of an individual's arms measured at the fingertips to the other when raised parallel to the ground at shoulder height at a one-hundred eighty degree angle).
Comments:
Reference: HP:0012771
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandReduced arm span (HP:0012770) 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:0012771HP:0012771Increased arm span0APC2 CL E G H1029724036ORPHA:821Sotos syndromeHP:0040281 - Very frequent1
HP:0012771HP:0012771Increased arm span0DLG4 CL E G H17422903OMIM:618793INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 62; MRD622
HP:0012771HP:0012771Increased arm span0FBN1 CL E G H22003603ORPHA:284979Neonatal Marfan syndromeHP:0040282 - Frequent1361
HP:0012771HP:0012771Increased arm span0NSD1 CL E G H6432414234ORPHA:821Sotos syndromeHP:0040281 - Very frequent544
HP:0012771HP:0012771Increased arm span0SETD2 CL E G H2907218420ORPHA:821Sotos syndromeHP:0040281 - Very frequent60
HP:0012771HP:0012771Increased arm span0TGFB3 CL E G H704311769OMIM:615582LOEYS-DIETZ SYNDROME 5; LDS585
HP:0012771HP:0012771Increased arm span0TRAPPC2 CL E G H639923068ORPHA:93284Spondyloepiphyseal dysplasia tardaHP:0040281 - Very frequent46


Genes (7) :APC2 DLG4 FBN1 NSD1 SETD2 TGFB3 TRAPPC2

Diseases (5) :ORPHA:821 OMIM:618793 ORPHA:284979 OMIM:615582 ORPHA:93284
 

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