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:
expandGenetic Diseases, X-Linked (D040181)
Parent Node:
expandTourette Syndrome (D005879)
..Starting node
..expandModifier, X-Linked, for Neurofunctional Defects (C564098)

       Child Nodes:



 Sister Nodes: 
..expandChronic Motor Tics (C563241)
..expandModifier, X-Linked, for Neurofunctional Defects (C564098)
   

Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
Term ID:7352
Name:Modifier, X-Linked, for Neurofunctional Defects
Definition:
Alternative IDs:
ParentIDs:MESH:D005879|MESH:D040181
TreeNumbers:C10.228.140.079.898/C564098 |C10.228.662.825.800/C564098 |C10.574.500.850/C564098 |C16.320.322/C564098 |C16.320.400.820/C564098 |F03.550.825.850/C564098
Synonyms:Tourette Syndrome, Modifier of
Slim Mappings:Genetic disease (inborn)|Mental disorder|Nervous system disease
Reference: MedGen: C564098
MeSH: C564098
OMIM: 309840;

Genes:
Phenotypes
1 HP:0001417X-linked inheritance
2 HP:0000707Abnormality of the nervous system
Disease Causing ClinVar Variants