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:
Sleep disturbance (HP:0002360)

Parent Node:
Insomnia (HP:0100785)

..Starting node
..Maintenance insomnia (HP:0031355)

Term ID:

31355

Name:

Maintenance insomnia

Synonym:

Waking up several times during the night

Definition:

Abnormal difficulty in staying asleep. Affected individuals tend to wake up at night and have difficulty returning to sleep.

Comments:

Reference:

HP:0031355

Genes and Diseases:

Child Nodes:

Sister Nodes:

Sleep onset insomnia (HP:0031354)

Terminal insomnia (HP:0031356)

Input	HPO ID	HPO term	Distance	Gene	Gene id entrez	HGNC ID	DiseaseId	DiseaseName
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0031355	HP:0031355	Maintenance insomnia	0	SATB1 CL E G H	6304	10541	OMIM:619229	KOHLSCHUTTER-TONZ SYNDROME-LIKE; KTZSL

Genes (1) :SATB1

Diseases (1) :OMIM:619229

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