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:
Abnormality of the autonomic nervous system (HP:0002270)

Parent Node:
Abnormal autonomic nervous system physiology (HP:0012332)

..Starting node
..Abnormal sudomotor regulation (HP:0012333)

Term ID:

12333

Name:

Abnormal sudomotor regulation

Synonym:

Sudomotor sympathetic dysfunction

Definition:

An abnormal regulation of the sweat glands by the sympathetic nervous system associated with abnormal perspiration.

Comments:

Reference:

HP:0012333

Genes and Diseases:

Child Nodes:

Sister Nodes:

Horner syndrome (HP:0002277)

obsolete Autonomic dysregulation (HP:0002271)

obsolete Dysautonomia (HP:0002459)

Orthostatic hypotension (HP:0001278)

Orthostatic tachycardia (HP:0012173)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0012333	HP:0012333	Abnormal sudomotor regulation	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.