Human Phenotype Ontology 
Grandparent Node:
expandAbnormality of the hand (HP:0001155)help
Parent Node:
expandAbnormal palm morphology (HP:0100871)help
..Starting node
..expandLong palm (HP:0011302)help
Term ID: 11302
Name: Long palm
Synonym: Long palm
Definition: For children from birth to 16 years of age the length of the palm is more than the 97th centile; or, the length of the palm appears relatively long compared to the finger length or the limb length.
Comments:
Reference: HP:0011302
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal skin morphology of the palm (HP:0040211) help
..expandBroad palm (HP:0001169) help
..expandNarrow palm (HP:0004283) help
..expandPalmar neurofibromas (HP:0007576) help
..expandShort palm (HP:0004279) 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:0011302HP:0011302Long palm0POR CL E G H54479208ORPHA:95699Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiencyHP:0040283 - Occasional76
HP:0011302HP:0011302Long palm0SLC2A10 CL E G H8103113444ORPHA:3342Arterial tortuosity syndromeHP:0040283 - Occasional178
HP:0011302HP:0011302Long palm0SMS CL E G H661111123OMIM:309583Mental retardation, X-linked, syndromic, Snyder-Robinson type.19
HP:0011302HP:0011302Long palm0UBE3B CL E G H8991013478OMIM:244450Kaufman oculocerebrofacial syndrome.13
HP:0011302HP:0011302Long palm0UPF3B CL E G H6510920439OMIM:300676MENTAL RETARDATION, X-LINKED, SYNDROMIC 14; MRXS1433


Genes (5) :POR SLC2A10 SMS UBE3B UPF3B

Diseases (5) :ORPHA:95699 ORPHA:3342 OMIM:309583 OMIM:244450 OMIM:300676
 

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