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:
expandAnemia, Hemolytic, Congenital (D000745)
Parent Node:
expandJaundice, Obstructive (D041781)
..Starting node
..expandAnemia, hereditary spherocytic hemolytic (C536356)

       Child Nodes:



 Sister Nodes: 
..expandAnemia, hereditary spherocytic hemolytic (C536356)
..expandJaundice, Familial Obstructive, of Infancy (C564118)
   

Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
Term ID:631
Name:Anemia, hereditary spherocytic hemolytic
Definition:
Alternative IDs:
ParentIDs:MESH:D000745|MESH:D041781
TreeNumbers:C15.378.071.141.150/C536356 |C16.320.070/C536356 |C23.550.429.500.755/C536356 |C23.888.885.375.500/C536356
Synonyms:Acholuric jaundice |Chronic acholuric jaundice |Congenital hemolytic jaundice |Debrie's familial haemolytic disease |Minkowski-Chauffard disease |Minkowski-Chauffard-Gänsslen syndrome |Minkowski-Chauffard haemolytic jaundice
Slim Mappings:Blood disease|Genetic disease (inborn)|Pathology (process)|Signs and symptoms
Reference: MedGen: C536356
MeSH: C536356
OMIM:

Genes:
Phenotypes
Disease Causing ClinVar Variants