Human Phenotype Ontology 
Grandparent Node:
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Abnormal hair quantity (HP:0011362)help
Parent Node:
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Hypertrichosis (HP:0000998)help
..Starting node
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Sacral hypertrichosis (HP:0004532)help
Term ID: 4532
Name: Sacral hypertrichosis
Synonym:
Definition: Excessive, increased hair growth located in the sacral region.
Comments:
Reference: HP:0004532
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAnterior cervical hypertrichosis (HP:0004535) help
..expandCongenital, generalized hypertrichosis (HP:0004540) help
..expandElbow hypertrichosis (HP:0004780) help
..expandFacial hypertrichosis (HP:0002219) help
..expandGeneralized hypertrichosis (HP:0004554) help
..expandLumbar hypertrichosis (HP:0011913) help
..expandThoracic hypertrichosis (HP:0011914) 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:0004532HP:0004532Sacral hypertrichosis0SPATA5 CL E G H16637818119ORPHA:457351Microcephaly-intellectual disability-sensorineural hearing loss-epilepsy-abnormal muscle tone syndromeHP:0040284 - Very rare19


Genes (1) :SPATA5

Diseases (1) :ORPHA:457351
 

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