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Usher syndrome type 1

disorder
SNOMED 232057003CUI C1568247

Overview

Source: MedlinePlus.gov, National Library of Medicine. Not a substitute for medical advice.

Signs & Symptoms

Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.

Involuntary, rapid, rhythmic eye movements
Always present (100%)HP:0000639
Visual loss
Always present (100%)HP:0000572
Abnormal cochlea morphology
Very frequent (80-99%)HP:0000375
Abnormal ERG
Very frequent (80-99%)HP:0000512
Blind spot
Very frequent (80-99%)HP:0000575
Difficulties with night vision
Very frequent (80-99%)HP:0000662
Retinitis pigmentosa
Very frequent (80-99%)HP:0000510
Sensorineural deafness
Very frequent (80-99%)HP:0000407
Abnormality of balance
Frequent (30-79%)HP:0002141
Decreased visual acuity
Frequent (30-79%)HP:0007663
Delayed motor milestones
Frequent (30-79%)HP:0001270
Interictal vestibular dysfunction
Frequent (30-79%)HP:0001751
Lens opacities
Frequent (30-79%)HP:0000518
Speech delay
Frequent (30-79%)HP:0000750
Tunnel vision
Frequent (30-79%)HP:0007994
Depression
Occasional (5-29%)HP:0000716
Excessive, persistent worry and fear
Occasional (5-29%)HP:0000739
Abolished electroretinogram
HP:0000550
Absent vestibular function
HP:0008555

Quick Facts

SNOMED CT
232057003
UMLS CUI
C1568247
Fully Specified Name
Usher syndrome type 1 (disorder)
Specialists
0
Diagnostic Biomarkers
0
HPO Phenotypes
19
Medical Disclaimer

This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.

Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.