Hearing Loss Disease Portal


 
Switch to table view
Most Common: Hearing Loss (D034381), Deafness (D003638), Sensorineural HL (D006319), Waardenburg Syndrome, Usher Syndromes
Disease Browser
Parent Node:
expand
Amino Acid Metabolism, Inborn Errors (D000592)
Parent Node:
expand
Cataract (D002386)
Parent Node:
expand
Hypertension (D006973)
Parent Node:
expand
Microphthalmos (D008850)
Parent Node:
expand
Seizures (D012640)
Parent Node:
expand
Tachycardia, Paroxysmal (D013614)
..Starting node
..expand
Adams Nance syndrome (C538224)

       Child Nodes:



 Sister Nodes: 
..expandAdams Nance syndrome (C538224)
   

Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
Term ID:253
Name:Adams Nance syndrome
Definition:
Alternative IDs:
ParentIDs:MESH:D000592|MESH:D002386|MESH:D006973|MESH:D008850|MESH:D012640|MESH:D013614
TreeNumbers:C10.228.140.490.631/C538224 |C10.597.742/C538224 |C11.250.566/C538224 |C11.510.245/C538224 |C14.280.067.845.695/C538224 |C14.907.489/C538224 |C16.131.384.666/C538224 |C16.320.565.100/C538224 |C18.452.648.100/C538224 |C23.550.073.845.695/C538224 |C23.888.592.742/C5
Synonyms:Tachycardia hypertension microphthalmos hyperglycinuria
Slim Mappings:Cardiovascular disease|Congenital abnormality|Eye disease|Genetic disease (inborn)|Metabolic disease|Nervous system disease|Pathology (process)|Signs and symptoms
Reference: MedGen: C538224
MeSH: C538224
OMIM:

Genes:
Phenotypes
Disease Causing ClinVar Variants