Hearing Loss Disease Portal


 
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Most Common: Hearing Loss (D034381), Deafness (D003638), Sensorineural HL (D006319), Waardenburg Syndrome, Usher Syndromes
Disease Browser
Parent Node:
expandNeurobehavioral Manifestations (D019954)
Parent Node:
expandPsychomotor Disorders (D011596)
..Starting node
..expandApraxias (D001072)

       Child Nodes:
........expandAlien Hand Syndrome (D055964)
........expandAlzheimer Disease, Familial, 3, with Spastic Paraparesis and Apraxia (C564330)
........expandApraxia, Ideomotor (D020240)
........expandEarly-onset ataxia with oculomotor apraxia and hypoalbuminemia (C538013)
........expandGait Apraxia (D020235)
........expandRolandic Epilepsy, Mental Retardation, And Speech Dyspraxia, Autosomal Dominant (C563392)
........expandRolandic Epilepsy, Mental Retardation, and Speech Dyspraxia, X-Linked (C564467)
........expandSpecific Language Impairment 4 (C567288)
........expandSPEECH-LANGUAGE DISORDER 1 (OMIM:602081)
........expandWieacker syndrome (C536703)



 Sister Nodes: 
..expandApraxias (D001072) Child10
..expandBowen-Conradi syndrome (C537081)
..expandC SYNDROME (OMIM:211750)
..expandCHROMOSOME 3pter-p25 DELETION SYNDROME (OMIM:613792)
..expandDe Hauwere Leroy Adriaenssens syndrome (C535991)
..expandDevelopmental Delay, Epilepsy, and Neonatal Diabetes (C565253)
..expandDiaminopentanuria (C565630)
..expandDystonia, Dopa-Responsive, due to Sepiapterin Reductase Deficiency (C562657)
..expandEdinburgh Malformation Syndrome (C563051)
..expandFumaric aciduria (C538191)
..expandGenitopatellar Syndrome (C565255)
..expandGrowth Retardation, Small and Puffy Hands and Feet, and Eczema (C565528)
..expandHypomyelination, Global Cerebral (C567847)
..expandIchthyosis prematurity syndrome (C536271)
..expandKozlowski Rafinski Klicharska syndrome (C537509)
..expandMacDermot Winter syndrome (C537714)
..expandMegarbane syndrome (C536145)
..expandMyelodysplasia, Immunodeficiency, Facial Dysmorphism, Short Stature, and Psychomotor Delay (C563345)
..expandPhosphoglycerate Dehydrogenase Deficiency (C566618)
..expandPhosphoserine Aminotransferase Deficiency (C567032)
..expandPolyhydramnios, Megalencephaly, And Symptomatic Epilepsy (C567020)
..expandPsychomotor Agitation (D011595) Child1
..expandTrigonobrachycephaly, Bulbous Bifid Nose, Micrognathia, and Abnormalities of the Hands and Feet (C564759)
   

Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
Term ID:832
Name:Apraxias
Definition:A group of cognitive disorders characterized by the inability to perform previously learned skills that cannot be attributed to deficits of motor or sensory function. The two major subtypes of this condition are ideomotor (see APRAXIA, IDEOMOTOR) and ideational apraxia, which refers to loss of the ability to mentally formulate the processes involved with performing an action. For example, dressing apraxia may result from an inability to mentally formulate the act of placing clothes on the body. Apraxias are generally associated with lesions of the dominant PARIETAL LOBE and supramarginal gyrus. (From Adams et al., Principles of Neurology, 6th ed, pp56-7)
Alternative IDs:
ParentIDs:MESH:D011596|MESH:D019954
TreeNumbers:C10.597.606.881.350 |C23.888.592.604.080 |C23.888.592.604.882.350
Synonyms:1, Speech-Language Disorder |1s, Speech-Language Disorder |Apraxia |Apraxia, Articulatory |Apraxia, Developmental Verbal |Apraxia, Dressing |Apraxia, Facial Oral |Apraxia, Facial-Oral |Apraxia, Gestural |Apraxia, Ideational |Apraxia, Motor |Apraxia of Phonation |Apr
Slim Mappings:Nervous system disease|Signs and symptoms
Reference: MedGen: D001072
MeSH: D001072
OMIM:

Genes:
Phenotypes
Disease Causing ClinVar Variants