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:
Sleep disturbance (HP:0002360)

Parent Node:
Sleep-wake cycle disturbance (HP:0006979)

..Starting node
..Late chronotype (HP:0031874)

Term ID:

31874

Name:

Late chronotype

Synonym:

Late sleep onset

Definition:

A tendency towards rising very late in the morning and going to bed late at night.

Comments:

Reference:

HP:0031874

Genes and Diseases:

Child Nodes:

Sister Nodes:

Early chronotype (HP:0031873)

Sleep-wake inversion (HP:0031849)

Input	HPO ID	HPO term	Distance	Gene	Gene id entrez	HGNC ID	DiseaseId	DiseaseName	ClinVar variants
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0031874	HP:0031874	Late chronotype	0	CHD8 CL E G H	57680	20153	OMIM:615032	AUTISM, SUSCEPTIBILITY TO, 18; AUTS18	72

Genes (1) :CHD8

Diseases (1) :OMIM:615032

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