Human Phenotype Ontology 
Grandparent Node:
expandAbnormality of skin adnexa morphology (HP:0011138)help
Parent Node:
expandAbnormal hair morphology (HP:0001595)help
..Starting node
..expandobsolete Abnormality of hair density (HP:0011357)help
Term ID: 11357
Name: obsolete Abnormality of hair density
Synonym:
Definition:
Comments:
Reference: HP:0011357
Genes and Diseases:
 
       Child Nodes:
........expandSparse hair (HP:0008070) help
................... HP:0000653 Sparse eyelashes
................... HP:0002209 Sparse scalp hair
................... HP:0002215 Sparse axillary hair
................... HP:0002225 Sparse pubic hair
................... HP:0002231 Sparse body hair
................... HP:0007464 Sparse facial hair
........expandThick hair (HP:0100874) help

 Sister Nodes: 
..expandAbnormal eyebrow morphology (HP:0000534) help
..expandAbnormal eyelash morphology (HP:0000499) help
..expandAbnormal hair pattern (HP:0010720) help
..expandAbnormal hair quantity (HP:0011362) help
..expandAbnormal hairshaft morphology (HP:0003328) help
..expandAbnormality of hair growth (HP:0040170) help
..expandAbnormality of hair pigmentation (HP:0009887) help
..expandAbnormality of hair texture (HP:0010719) help
..expandAbnormality of secondary sexual hair (HP:0009888) help
..expandAbnormality of the scalp hair (HP:0100037) help
..expandTrichodysplasia (HP:0002552) 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:0011357HP:0011357obsolete Abnormality of hair density0 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.