Usher Syndromes [Usherovy syndromy]

topical
8
Terms

Hallgrenův syndrom
Usherův syndrom
Usherův syndrom - typ I
Usherův syndrom - typ II
Usherův syndrom - typ III
Usherův syndrom typu 1
Usherův syndrom typu 2
Usherův syndrom typu 3
Usherův syndrom typu I
Usherův syndrom typu II
Usherův syndrom typu III

 

Deafness-Retinitis Pigmentosa Syndrome
Dystrophia Retinae Pigmentosa-Dysostosis Syndrome
Graefe-Usher Syndrome
Hallgren Syndrome
Retinitis Pigmentosa And Congenital Deafness
Retinitis Pigmentosa-Deafness Syndrome
Usher Syndrome
Usher Syndrome, Type 1
Usher Syndrome, Type 1A
Usher Syndrome, Type 3
Usher Syndrome, Type I
Usher Syndrome, Type I, French Variety
Usher Syndrome, Type II
Usher Syndrome, Type IId
Usher Syndrome, Type III
Usher's Syndrome

Persistent link   https://www.medvik.cz/link/D052245
Definition

Autosomal recessive hereditary disorders characterized by congenital SENSORINEURAL HEARING LOSS and RETINITIS PIGMENTOSA. Genetically and symptomatically heterogeneous, clinical classes include type I, type II, and type III. Their severity, age of onset of retinitis pigmentosa and the degree of vestibular dysfunction are variable.

DUI
D052245 MeSH Browser
CUI
M0483844
Previous indexing
Deafness (1972-2005); Hearing Loss, Sensorineural (1983-2005); Retinitis Pigmentosa (1972-2005); Syndrome (1972-2005)
History note
2006
Public note
2006

Allowable subheadings

BL
blood
CF
cerebrospinal fluid
CI
chemically induced
CL
classification
CO
complications
DI
diagnosis 2
DG
diagnostic imaging
DH
diet therapy
DT
drug therapy 1
EC
economics
EM
embryology
EN
enzymology
EP
epidemiology
EH
ethnology 1
ET
etiology 1
GE
genetics 5
HI
history
IM
immunology
ME
metabolism 1
MI
microbiology
MO
mortality
NU
nursing
PS
parasitology
PA
pathology
PP
physiopathology
PC
prevention & control
PX
psychology
RT
radiotherapy
RH
rehabilitation
SU
surgery
TH
therapy 3
UR
urine
VE
veterinary
VI
virology

C Diseases
C09 Otorhinolaryngologic Diseases 678
C09.218 Ear Diseases 316
C09.218.458 Hearing Disorders 1 299
C09.218.458.341 Hearing Loss 217
C09.218.458.341.186 Deafness 435
C09.218.458.341.186.500 Deaf-Blind Disorders 65
C09.218.458.341.186.500.250 CHARGE Syndrome 1
C09.218.458.341.186.500.500 Usher Syndromes 8
C09.218.458.341.186.500.750 Wolfram Syndrome 8
C09.218.458.341.887 Hearing Loss, Sensorineural 92
C09.218.458.341.887.432 Hearing Loss, Central 2
C09.218.458.341.887.460 Hearing Loss, Noise-Induced 107
C09.218.458.341.887.772 Presbycusis 33
C09.218.458.341.887.886 Usher Syndromes 8
C10 Nervous System Diseases 1 884
C10.597 Neurologic Manifestations 1 055
C10.597.751 Sensation Disorders 94
C10.597.751.418 Hearing Disorders 1 299
C10.597.751.418.341 Hearing Loss 217
C10.597.751.418.341.186 Deafness 435
C10.597.751.418.341.186.500 Deaf-Blind Disorders 65
C10.597.751.418.341.186.500.250 CHARGE Syndrome 1
C10.597.751.418.341.186.500.500 Usher Syndromes 8
C10.597.751.418.341.186.500.750 Wolfram Syndrome 8
C10.597.751.418.341.887 Hearing Loss, Sensorineural 92
C10.597.751.418.341.887.432 Hearing Loss, Central 2
C10.597.751.418.341.887.460 Hearing Loss, Noise-Induced 107
C10.597.751.418.341.887.772 Presbycusis 33
C10.597.751.418.341.887.886 Usher Syndromes 8
C10.597.751.941 Vision Disorders 710
C10.597.751.941.162 Blindness 425
C10.597.751.941.162.625 Deaf-Blind Disorders 65
C10.597.751.941.162.625.250 CHARGE Syndrome 1
C10.597.751.941.162.625.500 Usher Syndromes 8
C10.597.751.941.162.625.750 Wolfram Syndrome 8
C11 Eye Diseases 1 495
C11.768 Retinal Diseases 404
C11.768.585 Retinal Degeneration 75
C11.768.585.658 Retinal Dystrophies 6
C11.768.585.658.500 Retinitis Pigmentosa 56
C11.768.585.658.500.627 Kearns-Sayre Syndrome 11
C11.768.585.658.500.813 Usher Syndromes 8
C11.966 Vision Disorders 710
C11.966.075 Blindness 425
C11.966.075.375 Deaf-Blind Disorders 65
C11.966.075.375.250 CHARGE Syndrome 1
C11.966.075.375.500 Usher Syndromes 8
C11.966.075.375.750 Wolfram Syndrome 8
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities 439
C16.131 Congenital Abnormalities 1 753
C16.131.077 Abnormalities, Multiple 330
C16.131.077.299 Deaf-Blind Disorders 65
C16.131.077.299.250 CHARGE Syndrome 1
C16.131.077.299.500 Usher Syndromes 8
C16.131.077.299.750 Wolfram Syndrome 8
C16.320 Genetic Diseases, Inborn 1 215
C16.320.290 Eye Diseases, Hereditary 58
C16.320.290.684 Retinitis Pigmentosa 56
C16.320.290.684.249 Alstrom Syndrome 1
C16.320.290.684.500 Usher Syndromes 8
C23 Pathological Conditions, Signs and Symptoms 451
C23.888 Signs and Symptoms 3 919
C23.888.592 Neurologic Manifestations 1 055
C23.888.592.763 Sensation Disorders 94
C23.888.592.763.393 Hearing Disorders 1 299
C23.888.592.763.393.341 Hearing Loss 217
C23.888.592.763.393.341.887 Hearing Loss, Sensorineural 92
C23.888.592.763.393.341.887.432 Hearing Loss, Central 2
C23.888.592.763.393.341.887.460 Hearing Loss, Noise-Induced 107
C23.888.592.763.393.341.887.772 Presbycusis 33
C23.888.592.763.393.341.887.886 Usher Syndromes 8

Usher Syndrome, Type IC Disease MeSH Browser

Usher Syndrome, Type ID Disease MeSH Browser

Usher Syndrome, Type ID-F Disease MeSH Browser

Usher Syndrome, Type IE Disease MeSH Browser

Usher Syndrome, Type IF Disease MeSH Browser

Usher Syndrome, Type IG Disease MeSH Browser

Usher Syndrome, Type IH Disease MeSH Browser

Usher Syndrome, Type Ib Disease MeSH Browser

Usher syndrome, type 1B Disease MeSH Browser

Usher syndrome, type 1C Disease MeSH Browser

Usher syndrome, type 1D Disease MeSH Browser

Usher syndrome, type 1E Disease MeSH Browser

Usher syndrome, type 1F Disease MeSH Browser

Usher syndrome, type 2A Disease MeSH Browser

Usher syndrome, type 2B Disease MeSH Browser

Usher syndrome, type 2C Disease MeSH Browser

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