Human Phenotype Ontology

Hello! Guest! Please Login or Register! Clinician Mode

Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

Grandparent Node:
Abnormal hair morphology (HP:0001595)

Parent Node:
Abnormal hair quantity (HP:0011362)

..Starting node
..Anagen effluvium (HP:0025469)

Term ID:

25469

Name:

Anagen effluvium

Synonym:

Definition:

An abnormal loss of anagen (growth phase) hairs.

Comments:

Reference:

HP:0025469

Genes and Diseases:

Child Nodes:

Sister Nodes:

Absent hair (HP:0002298)

Alopecia (HP:0001596)

Hirsutism (HP:0001007)

Hypertrichosis (HP:0000998)

obsolete Hypotrichosis (HP:0001006)

Telogen effluvium (HP:0025470)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0025469	HP:0025469	Anagen effluvium	0	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.