Orphanet Rare Disease Ontology

Last uploaded: July 3, 2024
Preferred Name

Multiple epiphyseal dysplasia
Synonyms

Polyepiphyseal dysplasia

MED

EDM

Definitions

A rare group of primary bone dysplasia disorders characterized by the association of epiphyseal anomalies of long bones causing joint pain early in life, recurrent osteochondritis and early arthrosis. This group contains an heterogeneous group of diseases with variable expression. Common reported clinical signs include waddling gait and pain at onset, and moderate short stature. Some forms are mainly limited to the femoral epiphyses, while several other syndromes are characterized by the association of multiple epiphyseal dysplasia with other clinical manifestations such as myopia, deafness and facial dysmorphism. Diagnosis relies on identification of the radiological features.

ID

http://www.orpha.net/ORDO/Orphanet_251

alternative_term

Polyepiphyseal dysplasia

MED

EDM

definition

A rare group of primary bone dysplasia disorders characterized by the association of epiphyseal anomalies of long bones causing joint pain early in life, recurrent osteochondritis and early arthrosis. This group contains an heterogeneous group of diseases with variable expression. Common reported clinical signs include waddling gait and pain at onset, and moderate short stature. Some forms are mainly limited to the femoral epiphyses, while several other syndromes are characterized by the association of multiple epiphyseal dysplasia with other clinical manifestations such as myopia, deafness and facial dysmorphism. Diagnosis relies on identification of the radiological features.

definition_citation

Orphanet

expertlink

https://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=en&Expert=251

has_age_of_onset

Infancy

Neonatal

has_inheritance

Autosomal recessive

Autosomal dominant

hasDbXref

ICD-11:LD24.61

MedDRA:10028197

UMLS:C0026760

label

Multiple epiphyseal dysplasia

notation

Clinical group

ORPHA:251

prefixIRI

ORDO:Orphanet_251

prefLabel

Multiple epiphyseal dysplasia

present_in

Europe AND has_point_prevalence_average_value : 5.0 AND has_point_prevalence_range : 1-9 / 100 000

subClassOf

http://www.orpha.net/ORDO/Orphanet_557492

http://www.orpha.net/ORDO/Orphanet_93429

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Delete Mapping To Ontology Source
http://www.orpha.net/ORDO/Orphanet_251 CCONT SAME_URI
http://www.orpha.net/ORDO/Orphanet_251 EFO SAME_URI
http://www.orpha.net/ORDO/Orphanet_251 EFO SAME_URI
http://purl.obolibrary.org/obo/MONDO_0016648 CCONT LOOM
http://purl.obolibrary.org/obo/MONDO_0016648 HSPO LOOM
http://purl.obolibrary.org/obo/MONDO_0016648 EFO LOOM
http://purl.obolibrary.org/obo/MONDO_0016648 MONDO LOOM
http://purl.obolibrary.org/obo/MONDO_0016648 EFO LOOM
http://purl.obolibrary.org/obo/MONDO_0016648 DOVES LOOM
rgo:09485 GAMUTS LOOM
http://purl.bioontology.org/ontology/RCTV2/PG56.00 RCTV2 LOOM
http://purl.bioontology.org/ontology/MEDDRA/10028197 MEDDRA LOOM
http://www.phoc.org.cn/pmo/class/PMO_00013960 PMAPP-PMO LOOM
http://purl.obolibrary.org/obo/HP_0002654 HP LOOM
http://purl.obolibrary.org/obo/HP_0002654 UPHENO LOOM
http://purl.obolibrary.org/obo/HP_0002654 OBA LOOM
http://www.owl-ontologies.com/NPOntology.owl#DOID_12721 NATPRO LOOM
http://purl.obolibrary.org/obo/DOID_12721 DOID LOOM
http://purl.obolibrary.org/obo/DOID_12721 BAO LOOM
http://purl.obolibrary.org/obo/DOID_12721 HHEAR LOOM
http://purl.obolibrary.org/obo/DOID_12721 DDSS LOOM
http://purl.obolibrary.org/obo/DOID_12721 NIFSTD LOOM
http://purl.obolibrary.org/obo/DOID_12721 MIDO LOOM
http://purl.obolibrary.org/obo/DOID_12721 FNS-H LOOM
http://purl.bioontology.org/ontology/OMIM/MTHU037429 OMIM LOOM
http://purl.org/obo/owl/HP#HP_0002654 BDO LOOM
http://purl.jp/bio/4/id/200906023077216550 IOBC LOOM
http://purl.bioontology.org/ontology/ICD9CM/756.56 ICD9CM LOOM
http://www.semanticweb.org/ontologies/2012/11/abnormalities.owl#phenodb:1366 IFAR LOOM
http://purl.bioontology.org/ontology/SNMI/D4-00A41 SNMI LOOM
http://purl.bioontology.org/ontology/SNOMEDCT/59708000 SNOMEDCT LOOM
http://purl.bioontology.org/ontology/RCD/PG56. RCD LOOM
http://www.limics.org/hrdo/rdfns#pat_id_1809 HRDO LOOM
http://www.gamuts.net/entity#multiple_epiphyseal_dysplasia GAMUTS REST