Human Phenotype Ontology 
Grandparent Node:
expandAbnormality of prenatal development or birth (HP:0001197)help
Parent Node:
expandFetal ultrasound soft marker (HP:0011425)help
..Starting node
..expandFetal fifth finger clinodactyly (HP:0011431)help
Term ID: 11431
Name: Fetal fifth finger clinodactyly
Synonym: Fetal little finger curvature; Fetal pinkie finger curvature; Fetal pinky finger curvature; Foetal fifth finger clinodactyly; Foetal little finger curvature; Foetal pinkie finger curvature; Foetal pinky finger curvature
Definition: Fifth finger clinodactyly is defined by a hypoplastic or absent mid-phalanx of the fifth digit. Ultrasound identification of the fetal hand must first be undertaken and then appropriate magnification accomplished. The evaluation requires stretching of the 5 fingers. The diagnosis is established when the middle phalanx of the fifth finger is markedly smaller than normal or absent, which often causes the finger to be curved inward (PMID:16100637).
Comments:
Reference: HP:0011431
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbsence of stomach bubble on fetal sonography (HP:0010963) help
..expandEchogenic fetal bowel (HP:0010943) help
..expandEchogenic intracardiac focus (HP:0010942) help
..expandEnlarged fetal cisterna magna (HP:0011427) help
..expandFetal choroid plexus cysts (HP:0011426) help
..expandFetal pyelectasis (HP:0010945) help
..expandHypoplasia of fetal nasal bone (HP:0011430) help
..expandMild fetal ventriculomegaly (HP:0010952) help
..expandShort fetal femur length (HP:0011428) help
..expandShort fetal humerus length (HP:0011429) help
..expandSingle umbilical artery (HP:0001195) help
..expandThickened nuchal skin fold (HP:0000474) 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:0011431HP:0011431Fetal fifth finger clinodactyly0 CL E G H


Genes (0) :

Diseases (0) :
 

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