Human Phenotype Ontology

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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
..obsolete Hypotrichosis (HP:0001006)

Term ID:

1006

Name:

obsolete Hypotrichosis

Synonym:

Definition:

Comments:

Reference:

HP:0001006

Genes and Diseases:

Child Nodes:

........

Progressive hypotrichosis (HP:0002296)

........

Generalized hypotrichosis (HP:0004528)

........

Hypotrichosis of the scalp (HP:0004782)

Sister Nodes:

Absent hair (HP:0002298)

Alopecia (HP:0001596)

Anagen effluvium (HP:0025469)

Hirsutism (HP:0001007)

Hypertrichosis (HP:0000998)

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:0001006	HP:0001006	obsolete Hypotrichosis	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.