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:
expandFoot Deformities, Congenital (D005532)
Parent Node:
expandHand Deformities, Congenital (D006228)
Parent Node:
expandPierre Robin Syndrome (D010855)
Parent Node:
expandSyncope (D013575)
Parent Node:
expandVentricular Premature Complexes (D018879)
..Starting node
..expandStoll Alembik Dott syndrome (C537497)

       Child Nodes:



 Sister Nodes: 
..expandStoll Alembik Dott syndrome (C537497)
   

Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
Term ID:10677
Name:Stoll Alembik Dott syndrome
Definition:
Alternative IDs:
ParentIDs:MESH:D005532|MESH:D006228|MESH:D010855|MESH:D013575|MESH:D018879
TreeNumbers:C05.330.495/C537497 |C05.390.408/C537497 |C05.500.460.606/C537497 |C05.660.207.540.460.606/C537497 |C05.660.585.512.380/C537497 |C05.660.585.988.425/C537497 |C07.320.440.606/C537497 |C07.650.500.460.606/C537497 |C10.597.606.358.800.600/C537497 |C14.280.067.325.50
Synonyms:Ventricular extrasystoles with syncope, perodactyly, and robin sequence
Slim Mappings:Cardiovascular disease|Congenital abnormality|Mouth disease|Musculoskeletal disease|Nervous system disease|Pathology (process)|Signs and symptoms
Reference: MedGen: C537497
MeSH: C537497
OMIM:

Genes:
Phenotypes
Disease Causing ClinVar Variants