Human Phenotype Ontology 
Grandparent Node:
expand
Abnormal finger flexion creases (HP:0006143)help
Parent Node:
expand
Absent phalangeal crease (HP:0006109)help
..Starting node
..expand
Absent proximal finger flexion creases (HP:0006077)help
Term ID: 6077
Name: Absent proximal finger flexion creases
Synonym:
Definition: Absence of the proximal interphalangeal flexion creases of the fingers.
Comments:
Reference: HP:0006077
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbsent distal interphalangeal creases (HP:0001032) help
..expandSingle interphalangeal crease of fifth finger (HP:0006216) 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:0006077HP:0006077Absent proximal finger flexion creases0MET CL E G H42337029OMIM:620019375
HP:0006077HP:0006077Absent proximal finger flexion creases0NOG CL E G H92417866OMIM:186500Multiple synostoses syndrome 122
HP:0006077HP:0006077Absent proximal finger flexion creases0TBX15 CL E G H691311594OMIM:260660Cousin syndrome.5


Genes (3) :MET NOG TBX15

Diseases (3) :OMIM:620019 OMIM:186500 OMIM:260660
 

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