Human Phenotype Ontology 
Grandparent Node:
expandAbnormality of the nose (HP:0000366)help
Parent Node:
expandAbnormality of the nasolabial region (HP:0005289)help
..Starting node
..expandUnderdeveloped nasolabial fold (HP:0010801)help
Term ID: 10801
Name: Underdeveloped nasolabial fold
Synonym: Flat nasolabial fold; Nasolabial crease, hypoplastic; Nasolabial crease, underdeveloped; Nasolabial fold, hypoplastic; Shallow nasolabial fold
Definition: Reduced bulkiness of the crease or fold of skin running from the lateral margin of the nose, where nasal base meets the skin of the face, to a point just lateral to the corner of the mouth (cheilion or commissure).
Comments:
Reference: HP:0010801
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandProminent nasolabial fold (HP:0005272) 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:0010801HP:0010801Underdeveloped nasolabial fold0MAN1B1 CL E G H112536823ORPHA:397941MAN1B1-CDGHP:0040283 - Occasional93
HP:0010801HP:0010801Underdeveloped nasolabial fold0MAN1B1 CL E G H112536823OMIM:614202Rafiq syndrome93
HP:0010801HP:0010801Underdeveloped nasolabial fold0SNRPN CL E G H663811164ORPHA:177907Prader-Willi syndrome due to translocationHP:0040283 - Occasional37


Genes (2) :MAN1B1 SNRPN

Diseases (3) :ORPHA:397941 OMIM:614202 ORPHA:177907
 

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