Home Contact Sitemap

PedAM

Pediatric Disease Annotations & Medicines



   mutism
  

Disease ID 1849
Disease mutism
Definition
The inability to generate oral-verbal expression, despite normal comprehension of speech. This may be associated with BRAIN DISEASES or MENTAL DISORDERS. Organic mutism may be associated with damage to the FRONTAL LOBE; BRAIN STEM; THALAMUS; and CEREBELLUM. Selective mutism is a psychological condition that usually affects children characterized by continuous refusal to speak in social situations by a child who is able and willing to speak to selected persons. Kussmal aphasia refers to mutism in psychosis. (From Fortschr Neurol Psychiatr 1994; 62(9):337-44)
Synonym
inability to speak
muteness
mutism (finding)
mutism [disease/finding]
mutisms
DOID
UMLS
C0026884
MeSH
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:18)
C0036341  |  schizophrenia  |  3
C0018784  |  sensorineural deafness  |  2
C0036349  |  paranoid schizophrenia  |  2
C0497327  |  dementia  |  2
C0155550  |  neural deafness  |  2
C0004134  |  ataxia  |  2
C0007789  |  cerebral palsy  |  1
C0743039  |  progressive dementia  |  1
C0025149  |  medulloblastoma  |  1
C0034372  |  quadriplegia  |  1
C0041341  |  tuberous sclerosis  |  1
C0008049  |  chicken pox  |  1
C0014038  |  encephalitis  |  1
C0018991  |  hemiplegia  |  1
C0041341  |  tuberous sclerosis complex  |  1
C0003467  |  anxiety  |  1
C0014059  |  acute disseminated encephalomyelitis  |  1
C0021400  |  influenza  |  1
Curated Gene(Waiting for update.)
Inferring Gene(Waiting for update.)
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:49)
2896  |  GRN  |  DISEASES
3784  |  KCNQ1  |  DISEASES
6343  |  SCT  |  DISEASES
1738  |  DLD  |  DISEASES
92797  |  HELB  |  DISEASES
1890  |  TYMP  |  DISEASES
4659  |  PPP1R12A  |  DISEASES
3757  |  KCNH2  |  DISEASES
23523  |  CABIN1  |  DISEASES
23476  |  BRD4  |  DISEASES
492  |  ATP2B3  |  DISEASES
10190  |  TXNDC9  |  DISEASES
5286  |  PIK3C2A  |  DISEASES
5860  |  QDPR  |  DISEASES
7471  |  WNT1  |  DISEASES
57465  |  TBC1D24  |  DISEASES
6010  |  RHO  |  DISEASES
6469  |  SHH  |  DISEASES
3251  |  HPRT1  |  DISEASES
9317  |  PTER  |  DISEASES
3611  |  ILK  |  DISEASES
478  |  ATP1A3  |  DISEASES
7200  |  TRH  |  DISEASES
1816  |  DRD5  |  DISEASES
3350  |  HTR1A  |  DISEASES
3291  |  HSD11B2  |  DISEASES
5663  |  PSEN1  |  DISEASES
6331  |  SCN5A  |  DISEASES
6900  |  CNTN2  |  DISEASES
23583  |  SMUG1  |  DISEASES
4137  |  MAPT  |  DISEASES
875  |  CBS  |  DISEASES
10019  |  SH2B3  |  DISEASES
8310  |  ACOX3  |  DISEASES
617  |  BCS1L  |  DISEASES
79947  |  DHDDS  |  DISEASES
26047  |  CNTNAP2  |  DISEASES
9211  |  LGI1  |  DISEASES
1025  |  CDK9  |  DISEASES
64344  |  HIF3A  |  DISEASES
2706  |  GJB2  |  DISEASES
2737  |  GLI3  |  DISEASES
55120  |  FANCL  |  DISEASES
1994  |  ELAVL1  |  DISEASES
93986  |  FOXP2  |  DISEASES
3267  |  AGFG1  |  DISEASES
5424  |  POLD1  |  DISEASES
10687  |  PNMA2  |  DISEASES
102723508  |  KANTR  |  DISEASES
Locus(Waiting for update.)
Disease ID 1849
Disease mutism
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:29)
HP:0002063  |  Muscle rigidity  |  4
HP:0100753  |  Schizophrenia  |  3
HP:0000726  |  Dementia  |  2
HP:0000407  |  sensorineural hearing loss  |  2
HP:0001251  |  Ataxia  |  2
HP:0001298  |  Encephalopathy  |  2
HP:0008625  |  Severe sensorineural deafness  |  2
HP:0000365  |  Hearing impairment  |  2
HP:0001260  |  Dysarthric speech  |  2
HP:0001336  |  Myoclonic jerks  |  2
HP:0001268  |  Mental deterioration  |  1
HP:0001297  |  Cerebral vascular events  |  1
HP:0000708  |  Behavioral problems  |  1
HP:0012671  |  Abulia  |  1
HP:0002533  |  Abnormal posturing  |  1
HP:0002301  |  Hemiplegia  |  1
HP:0000605  |  Supranuclear gaze paralysis  |  1
HP:0000739  |  Anxiety  |  1
HP:0001249  |  Mental retardation  |  1
HP:0006846  |  Acute encephalopathy  |  1
HP:0000511  |  Vertical supranuclear gaze palsy  |  1
HP:0100021  |  Cerebral palsy  |  1
HP:0030223  |  Perseveration  |  1
HP:0002067  |  Bradykinesia  |  1
HP:0002304  |  Akinesia  |  1
HP:0002445  |  Paralysis of all four limbs  |  1
HP:0001575  |  Mood alterations  |  1
HP:0002885  |  Medulloblastoma  |  1
HP:0000713  |  Agitation  |  1
Disease ID 1849
Disease mutism
Manually Symptom(Waiting for update.)
Text Mined Symptom(Waiting for update.)
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
All Snps(Total Genotypes:0)
(Waiting for update.)
GWASdb Annotation(Total Genotypes:0)
(Waiting for update.)
GWASdb Snp Trait(Total Genotypes:0)
(Waiting for update.)
Mapped by lexical matching(Total Items:0)
(Waiting for update.)
Mapped by homologous gene(Total Items:0)
(Waiting for update.)
Chemical(Total Drugs:7)
CUI ChemicalName ChemicalID CasRN DiseaseName DiseaseID DirectEvidence PubMedIDs
C0026884chlorpromazineD00274650-53-3mutismMESH:D009155marker/mechanism4405372
C0026884ifosfamideD0070693778-73-2mutismMESH:D009155marker/mechanism12035842
C0026884mesnaD01508019767-45-4mutismMESH:D009155marker/mechanism3098318
C0026884methadoneD00869176-99-3mutismMESH:D009155marker/mechanism17187532
C0026884methotrexateD0087271959/5/2mutismMESH:D009155marker/mechanism11966594
C0026884phenytoinD01067257-41-0mutismMESH:D009155marker/mechanism7816230
C0026884tacrolimusD016559109581-93-3mutismMESH:D009155marker/mechanism11014653
FDA approved drug and dosage information(Total Drugs:0)
(Waiting for update.)
FDA labeling changes(Total Drugs:0)
(Waiting for update.)