MCID: VRB001
MIFTS: 18

Verbal Auditory Agnosia

Categories: Ear diseases, Mental diseases

Aliases & Classifications for Verbal Auditory Agnosia

MalaCards integrated aliases for Verbal Auditory Agnosia:

Name: Verbal Auditory Agnosia 12 15

Classifications:



External Ids:

Disease Ontology 12 DOID:0060154

Summaries for Verbal Auditory Agnosia

Disease Ontology : 12 An agnosia that is a loss of the ability to recognising spoken words as semantically meaningful.

MalaCards based summary : Verbal Auditory Agnosia is related to auditory agnosia and landau-kleffner syndrome. An important gene associated with Verbal Auditory Agnosia is SCNM1 (Sodium Channel Modifier 1). Affiliated tissues include brain, cortex and temporal lobe.

Wikipedia : 74 Auditory verbal agnosia (AVA), also known as pure word deafness, is the inability to comprehend speech.... more...

Related Diseases for Verbal Auditory Agnosia

Diseases related to Verbal Auditory Agnosia via text searches within MalaCards or GeneCards Suite gene sharing:

(show top 50) (show all 54)
# Related Disease Score Top Affiliating Genes
1 auditory agnosia 31.0 SRPX2 GABRG2
2 landau-kleffner syndrome 30.2 SRPX2 GABRG2 ELP4
3 seizure disorder 29.3 SCN1B GABRG2 CPA6
4 agnosia 10.7
5 epilepsy, focal, with speech disorder and with or without mental retardation 10.4
6 branchiootic syndrome 1 10.4
7 aphasia 10.4
8 macrocephaly/megalencephaly syndrome, autosomal recessive 10.1
9 expressive language disorder 10.1
10 brain injury 10.1
11 megalencephaly 10.1
12 traumatic brain injury 10.1
13 reflex epilepsy 10.0 SCNM1 GABRG2
14 band heterotopia 10.0 SRPX2 ARX
15 febrile seizures, familial, 11 9.9 GABRG2 CPA6
16 speech disorder 9.9 SRPX2 ELP4
17 infancy electroclinical syndrome 9.8 SCN1B ARX
18 febrile seizures, familial, 6 9.8 SCN1B GABRG2
19 febrile seizures, familial, 5 9.8 SCN1B GABRG2
20 febrile seizures, familial, 2 9.8 SCN1B GABRG2
21 febrile seizures, familial, 1 9.8 SCN1B GABRG2
22 early onset absence epilepsy 9.8 SCN1B GABRG2
23 generalized epilepsy with febrile seizures plus, type 2 9.8 SCN1B GABRG2
24 generalized epilepsy with febrile seizures plus, type 1 9.8 SCN1B GABRG2
25 febrile seizures, familial, 8 9.8 SCN1B GABRG2
26 febrile seizures, familial, 4 9.8 SCN1B GABRG2
27 epilepsy, nocturnal frontal lobe, 1 9.8 SCN1B GABRG2
28 epilepsy with generalized tonic-clonic seizures 9.8 SCN1B GABRG2
29 generalized epilepsy with febrile seizures plus, type 7 9.7 SCN1B GABRG2
30 focal epilepsy 9.7 GABRG2 CPA6
31 adolescence-adult electroclinical syndrome 9.7 SCN1B GABRG2
32 photosensitive epilepsy 9.7 SCN1B GABRG2
33 benign familial neonatal epilepsy 9.7 SCN1B GABRG2
34 epilepsy, familial temporal lobe, 1 9.7 SCN1B GABRG2
35 unverricht-lundborg syndrome 9.7 SCN1B GABRG2
36 benign familial infantile epilepsy 9.7 SCN1B GABRG2
37 periventricular nodular heterotopia 9.7 SRPX2 ARX
38 familial febrile seizures 9.7 SCN1B GABRG2
39 autosomal dominant nocturnal frontal lobe epilepsy 9.6 SCN1B GABRG2
40 temporal lobe epilepsy 9.6 SCN1B CPA6
41 electroclinical syndrome 9.6 SCN1B GABRG2 ARX
42 neonatal period electroclinical syndrome 9.6 SCN1B GABRG2 ARX
43 lennox-gastaut syndrome 9.6 SCN1B GABRG2 ARX
44 early myoclonic encephalopathy 9.5 SCN1B GABRG2 ARX
45 generalized epilepsy with febrile seizures plus 9.5 SCN1B GABRG2 ARX
46 epilepsy, familial temporal lobe, 5 9.5 SCN1B GABRG2 CPA6
47 febrile seizures 9.5 SCN1B GABRG2 CPA6
48 epilepsy, myoclonic juvenile 9.5 SCN1B GABRG2 CPA6
49 west syndrome 9.5 SCN1B GABRG2 ARX
50 dravet syndrome 9.4 SCNM1 SCN1B GABRG2 ARX

Graphical network of the top 20 diseases related to Verbal Auditory Agnosia:



Diseases related to Verbal Auditory Agnosia

Symptoms & Phenotypes for Verbal Auditory Agnosia

Drugs & Therapeutics for Verbal Auditory Agnosia

Search Clinical Trials , NIH Clinical Center for Verbal Auditory Agnosia

Genetic Tests for Verbal Auditory Agnosia

Anatomical Context for Verbal Auditory Agnosia

MalaCards organs/tissues related to Verbal Auditory Agnosia:

40
Brain, Cortex, Temporal Lobe

Publications for Verbal Auditory Agnosia

Articles related to Verbal Auditory Agnosia:

(show all 38)
# Title Authors PMID Year
1
Music processing deficits in Landau-Kleffner syndrome: Four case studies in adulthood. 61
32442777 2020
2
Verbal auditory agnosia in a patient with traumatic brain injury: A case report. 61
29538212 2018
3
Auditory agnosia. 61
25726291 2015
4
Episodic epileptic verbal auditory agnosia in Landau Kleffner syndrome treated with combination diazepam and corticosteroids. 61
24453158 2014
5
Landau-Kleffner syndrome: a study of 29 patients. 61
24315829 2014
6
The speech aversion hypothesis has explanatory power in a Minimal Speech Approach to aloof, non-verbal, severe autism. 61
22004986 2012
7
Changing perspectives on Landau-Kleffner syndrome. 61
21955111 2011
8
Benign childhood seizure susceptibility syndrome: three case reports. 61
21628136 2011
9
Pure word deafness associated with extrapontine myelinolysis. 61
21043052 2010
10
Landau-Kleffner syndrome: long-term follow-up. 61
18930363 2009
11
[Focal brain lesions and language dysfunction]. 61
17966959 2007
12
[Clinical characteristics and long-term prognosis of Landau-Kleffner syndrome]. 61
16624025 2006
13
Management of Landau-Kleffner syndrome. 61
16356025 2005
14
[Landau-Kleffner syndrome (acquired epileptic aphasia)]. 61
12529574 2003
15
Auditory perception in auditory neuropathy: clinical similarity with auditory verbal agnosia. 61
11934521 2002
16
[Clinical forms of infantile dysphasias]. 61
12447799 2002
17
Landau-Kleffner syndrome: a case of a dissociation between spoken and written language. 61
11889967 2001
18
Perception of dynamic acoustic patterns by an individual with unilateral verbal auditory agnosia. 61
10860565 2000
19
The influence of premorbid language skills and behavior on language recovery in children with verbal auditory agnosia. 61
10641609 2000
20
[Acquired epileptic aphasia]. 61
10637836 1999
21
Autistic regression with rolandic spikes. 61
10456804 1999
22
A case of verbal auditory agnosia: missing the word ... missing the sound.... 61
10343694 1998
23
Brain single photon emission computed tomography imaging in Landau-Kleffner syndrome. 61
8603627 1996
24
Electrophysiologic manifestations of impaired temporal lobe auditory processing in verbal auditory agnosia. 61
8719073 1995
25
[Verbal auditory agnosia: SPECT study of the brain]. 61
8556589 1995
26
Verbal auditory agnosia with focal EEG abnormality: an unusual case of a child presenting to an ENT surgeon with "deafness". 61
7798001 1995
27
Sanfilippo type D presenting with acquired language disorder but without features of mucopolysaccharidosis. 61
7822734 1994
28
Diazepam therapy of verbal auditory agnosia. 61
8358596 1993
29
Regional cerebral perfusion in Landau-Kleffner syndrome and related childhood aphasias. 61
1383478 1992
30
[Non-verbal auditory agnosia with EEG abnormalities and epilepsy; an unusual case of Landau-Kleffner syndrome]. 61
1375480 1992
31
Autistic and dysphasic children. II: Epilepsy. 61
1956740 1991
32
Landau-Kleffner syndrome: epileptic activity in the auditory cortex. 61
1716495 1991
33
Verbal auditory agnosia in children. 61
3229568 1988
34
Pure word deafness (acquired verbal auditory agnosia) in an Arabic speaking patient. 61
3378145 1988
35
Syndromes in developmental dysphasia and adult aphasia. 61
2451853 1988
36
The Landau-Kleffner syndrome of acquired epileptic aphasia: unusual clinical outcome, surgical experience, and absence of encephalitis. 61
2447519 1988
37
Verbal auditory agnosia in children. 61
870358 1977
38
Congenital verbal-auditory agnosia (Word Deafness). 61
14807659 1951

Variations for Verbal Auditory Agnosia

Expression for Verbal Auditory Agnosia

Search GEO for disease gene expression data for Verbal Auditory Agnosia.

Pathways for Verbal Auditory Agnosia

GO Terms for Verbal Auditory Agnosia

Sources for Verbal Auditory Agnosia

3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
17 EFO
18 ExPASy
19 FMA
20 GARD
28 GO
29 GTR
30 HMDB
31 HPO
32 ICD10
33 ICD10 via Orphanet
34 ICD9CM
35 IUPHAR
36 KEGG
37 LifeMap
39 LOVD
41 MedGen
44 MeSH
45 MESH via Orphanet
46 MGI
49 NCI
50 NCIt
51 NDF-RT
53 NINDS
54 Novoseek
56 OMIM via Orphanet
57 OMIM® (Updated 05-Mar-2021)
61 PubMed
63 QIAGEN
68 SNOMED-CT via HPO
69 TGDB
70 Tocris
71 UMLS
72 UMLS via Orphanet
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