raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:93445

OBSOLETE: Bone disease with increased bone density and metaphyseal or diaphyseal involvement

inactive · referred to ORPHA:93444Primary bone dysplasia with increased bone density

Type
Category
Group
Group of disorders
Status
inactive
Flag
Obsolete entity

This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.<br/><br/>Instead, consider using Primary bone dysplasia with increased bone density

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Bone disease with increased bone density and metaphyseal or diaphyseal involvement
frOBSOLETE : Maladie osseuse condensante avec atteinte diaphysaire et métaphysaire
deOBSOLET: Knochendichte, erhöhte, mit metaphysärer oder diaphysärer Beteiligung
esOBSOLETO: Aumento de la densidad ósea con afectación metafisaria o diafisaria.
itOBSOLETO: Aumento della densità ossea con coinvolgimento metafisario e diafisario
nlOBSOLEET: Botziekte met verhoogde botdichtheid en metafysaire of diafysaire betrokkenheid
ptOBSOLETO: Doença óssea com aumento da densidade óssea e envolvimento metafisiário ou diafisiário
plNIEAKTUALNE: Choroba kosci ze zwiekszona gestoscia w przynasadach lub trzonie
csNEAKTUÁLNÍ: Kostní onemocnění se zvýšenou hustotou kostí a postižením metafýzy nebo diafýzy
ukЗАСТАРІЛО: Захворювання кісток з підвищеною щільністю кісткової тканини та метафізарним або діафізарним ураженням
zh弃用:骨病伴骨密度增加并累及干骺端或骨干
trEski adı: Artmış kemik yoğunluğu ve metafiz veya diyafiz tutulumu olan kemik hastalığı
2

Cross-references

qualifier = Orphanet mapping relation

No cross-references in this release.

3

Classification

Not placed in any Orphanet classification in this release.

No children.

4

Genes

0 direct

Orphanet records no gene directly on this code.

5

Prevalence and incidence

0 records

No prevalence record in this release.

6

HPO phenotypes

Orphanet has no HPO annotation for this code in this release.

7

Sources for this card