Phenotype Library | Search Phenotypes

Hereditary Multiple Osteochondromas (MONDO:0005508)

A bone neoplasm characterized by development of two or more cartilage capped bony outgrowths (osteochondromas) of the long bones.

Overview

Category

Ontology ID

Internal:7164

Synonyms

Bessel-Hagen disease

exostoses, multiple

multiple cartilaginous exostoses

osteochondromatosis syndrome

osteochondromatosis syndrome (disorder) [ambiguous]

hereditary multiple exostoses 1

hereditary multiple exostoses 2

hereditary multiple exostoses 3

EXT

HMO

hereditary multiple exostoses

hereditary multiple exostosis

multiple exostoses

Mapped terms

DOID:206

GARD:0007035

MEDGEN:4612

MESH:D005097

NANDO:2200049

NANDO:2201014

NANDO:2201015

NCIT:C5183

NORD:1233

OMIMPS:133700

Orphanet:321

SCTID:254044004

SCTID:716742001

UMLS:C0015306

icd11.foundation:146330302

icd11.foundation:1578364807

Child terms