Preferred Name

hereditary spherocytosis

Synonyms

spherocytic anemia

hereditary spherocytosis

Minkowski Chauffard syndrome

Minkowski-Chauffard disease

congenital spherocytic hemolytic anemia

congenital spherocytosis

Definitions

Hereditary spherocytosis is a congenital hemolytic anemia with a wide clinical spectrum (from symptom-free carriers to severe hemolysis) characterized by anemia, variable jaundice, splenomegaly and cholelithiasis.

ID

http://purl.obolibrary.org/obo/MONDO_0019350

has_exact_synonym

spherocytic anemia

hereditary spherocytosis

Minkowski Chauffard syndrome

Minkowski-Chauffard disease

congenital spherocytic hemolytic anemia

has_related_synonym

congenital spherocytosis

label

hereditary spherocytosis

prefixIRI

MONDO:0019350

prefLabel

hereditary spherocytosis

seeAlso

https://rarediseases.info.nih.gov/diseases/6639/hereditary-spherocytosis

textual definition

Hereditary spherocytosis is a congenital hemolytic anemia with a wide clinical spectrum (from symptom-free carriers to severe hemolysis) characterized by anemia, variable jaundice, splenomegaly and cholelithiasis.

subClassOf

http://purl.obolibrary.org/obo/MONDO_0003689

Delete Subject Author Type Created
No notes to display
Create mapping

Delete Mapping To Ontology Source
http://purl.obolibrary.org/obo/MONDO_0019350 MONDO SAME_URI
http://purl.obolibrary.org/obo/MONDO_0019350 EFO SAME_URI
http://purl.obolibrary.org/obo/MONDO_0019350 MONDO SAME_URI
http://purl.obolibrary.org/obo/MONDO_0019350 MONDO LOOM
http://nanbyodata.jp/ontology/NANDO_2200622 NANDO LOOM
http://purl.bioontology.org/ontology/MEDDRA/10019904 MEDDRA LOOM
http://purl.bioontology.org/ontology/SNOMEDCT/55995005 SNOMEDCT LOOM
http://purl.bioontology.org/ontology/ICD9CM/282.0 ICD9CM LOOM
http://sbmi.uth.tmc.edu/ontology/ochv#C0037889 OCHV LOOM
http://purl.bioontology.org/ontology/CSP/0427-1870 CRISP LOOM
http://purl.bioontology.org/ontology/RCD/D100. RCD LOOM
http://purl.obolibrary.org/obo/DOID_12971 CLO LOOM
http://purl.obolibrary.org/obo/DOID_12971 DOID LOOM
http://purl.obolibrary.org/obo/DOID_12971 BAO LOOM
http://purl.obolibrary.org/obo/DOID_12971 HHEAR LOOM
http://purl.obolibrary.org/obo/DOID_12971 NIFSTD LOOM
http://purl.obolibrary.org/obo/DOID_12971 MIDO LOOM
http://purl.obolibrary.org/obo/DOID_12971 FNS-H LOOM
http://purl.bioontology.org/ontology/ICD10/D58.0 ICD10 LOOM
http://purl.bioontology.org/ontology/RCTV2/D100.00 RCTV2 LOOM
http://www.owl-ontologies.com/NPOntology.owl#DOID_12971 NATPRO LOOM
http://purl.bioontology.org/ontology/ICD10CM/D58.0 ICD10CM LOOM
http://purl.bioontology.org/ontology/ICPC2P/B78006 ICPC2P LOOM
http://purl.obolibrary.org/obo/MONDO_0019350 EFO LOOM
http://purl.obolibrary.org/obo/MONDO_0019350 MONDO LOOM
http://purl.obolibrary.org/obo/NCIT_C97074 BERO LOOM
http://www.orpha.net/ORDO/Orphanet_822 ORDO LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#Hereditary_Spherocytosis CSEO LOOM
http://www.gamuts.net/entity#hereditary_spherocytosis GAMUTS LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C97074 NCIT LOOM
http://www.limics.org/hrdo/rdfns#pat_id_3252 HRDO LOOM
http://www.owl-ontologies.com/unnamed.owl#RID15049 DERMLEX LOOM