Experimental Factor Ontology

Last uploaded: June 18, 2024
Preferred Name

mucopolysaccharidosis

Synonyms

Mucopolysaccharidoses

mucopolysaccharidosis

mucopolysaccharidoses

MPS

Definitions

A group of autosomal recessive or X-linked inherited lysosomal storage disorders affecting the metabolism of mucopolysaccharides, resulting in the accumulation of mucopolysaccharides in the body. Signs and symptoms include organomegaly, mental retardation, abnormal skeletal development, heart disorders, hearing loss, and central nervous system deficiencies.

ID

http://purl.obolibrary.org/obo/MONDO_0019249

closeMatch

http://identifiers.org/meddra/10028093

database_cross_reference

icd11.foundation:1596128696

Orphanet:79213

OMIMPS:607014

NCIT:C61259

MedDRA:10028093

UMLS:C0026703

MESH:D009083

SCTID:11380006

DOID:12798

GARD:7065

ICD9:277.5

NORD:1461

definition

A group of autosomal recessive or X-linked inherited lysosomal storage disorders affecting the metabolism of mucopolysaccharides, resulting in the accumulation of mucopolysaccharides in the body. Signs and symptoms include organomegaly, mental retardation, abnormal skeletal development, heart disorders, hearing loss, and central nervous system deficiencies.

exactMatch

http://identifiers.org/mesh/D009083

http://purl.obolibrary.org/obo/DOID_12798

http://identifiers.org/snomedct/11380006

http://purl.obolibrary.org/obo/NCIT_C61259

http://linkedlifedata.com/resource/umls/id/C0026703

https://omim.org/phenotypicSeries/PS607014

http://purl.obolibrary.org/obo/Orphanet_79213

has_exact_synonym

Mucopolysaccharidoses

mucopolysaccharidosis

mucopolysaccharidoses

has_related_synonym

MPS

id

MONDO:0019249

in_subset

http://purl.obolibrary.org/obo/mondo/mondo-base#rare

http://purl.obolibrary.org/obo/mondo/mondo-base#otar

http://purl.obolibrary.org/obo/mondo/mondo-base#gard_rare

http://purl.obolibrary.org/obo/mondo/mondo-base#ordo_group_of_disorders

http://purl.obolibrary.org/obo/mondo/mondo-base#disease_grouping

http://purl.obolibrary.org/obo/mondo/mondo-base#nord_rare

label

mucopolysaccharidosis

notation

MONDO:0019249

prefLabel

mucopolysaccharidosis

see also

https://rarediseases.info.nih.gov/diseases/7065/mucopolysaccharidosis

subClassOf

http://purl.obolibrary.org/obo/MONDO_0002561

http://purl.obolibrary.org/obo/MONDO_0019214

http://purl.obolibrary.org/obo/MONDO_0015327

http://purl.obolibrary.org/obo/MONDO_0100365

Delete Subject Author Type Created
No notes to display
Create mapping

Delete Mapping To Ontology Source
http://purl.obolibrary.org/obo/MONDO_0019249 MONDO SAME_URI
http://purl.obolibrary.org/obo/MONDO_0019249 DOVES SAME_URI
http://purl.obolibrary.org/obo/MONDO_0019249 MONDO LOOM
http://www.owl-ontologies.com/NPOntology.owl#DOID_12798 NATPRO LOOM
http://www.co-ode.org/ontologies/galen#Mucopolysaccharidosis GALEN LOOM
http://purl.bioontology.org/ontology/SNOMEDCT/11380006 SNOMEDCT LOOM
http://purl.obolibrary.org/obo/MONDO_0019249 DOVES LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#Mucopolysaccharidosis CSEO LOOM
http://purl.bioontology.org/ontology/MEDDRA/10028093 MEDDRA LOOM
http://purl.obolibrary.org/obo/DOID_12798 CLO LOOM
http://purl.obolibrary.org/obo/DOID_12798 DTO LOOM
http://purl.obolibrary.org/obo/DOID_12798 BAO LOOM
http://purl.obolibrary.org/obo/DOID_12798 HHEAR LOOM
http://purl.obolibrary.org/obo/DOID_12798 NIFSTD LOOM
http://purl.obolibrary.org/obo/DOID_12798 FNS-H LOOM
http://www.limics.org/hrdo/rdfns#pat_id_11239 HRDO LOOM
http://purl.bioontology.org/ontology/CSP/1849-6106 CRISP LOOM
http://purl.bioontology.org/ontology/RCD/XE11o RCD LOOM
http://purl.obolibrary.org/obo/NCIT_C61259 BERO LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C61259 NCIT LOOM
http://sbmi.uth.tmc.edu/ontology/ochv#C0026703 OCHV LOOM
http://www.gamuts.net/entity#mucopolysaccharidosis GAMUTS LOOM
http://purl.obolibrary.org/obo/DERMO_0002677 DERMO LOOM
http://www.orpha.net/ORDO/Orphanet_79213 ORDO LOOM
http://www.owl-ontologies.com/Ontology1358660052.owl#Mucopolysaccharidosis PEDTERM LOOM
http://purl.bioontology.org/ontology/RCTV2/C375.00 RCTV2 LOOM
http://purl.bioontology.org/ontology/ICD9CM/277.5 ICD9CM LOOM
http://radlex.org/RID/RID34619 RADLEX LOOM
http://purl.obolibrary.org/obo/DOID_12798 DOID LOOM