raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:684290

Hypertrophic olivary degeneration

Synonyms: HOD

Type
Disease
Group
Disorder
Inheritance
Not applicable
Status
active

Orphadata ships no English definition for this code.

1

Names in Orphadata languages

9 of 12 languages
LangNameSynonyms
enHypertrophic olivary degenerationHOD
frDégénérescence olivaire hypertrophiqueDOH · Dégénérescence hypertrophique de l'olive bulbaire
deHypertrophe oliväre DegenerationHOD · Hypertrophe Degeneration des Nucleus olivaris
esDegeneración olivar hipertróficaDOH
itDegenerazione olivare ipertrofica= en
nlHypertrofe degeneratie van olivaHOD · Hypertrofe degeneratie van olijfvormig lichaam
ptDegeneração hipertrófica da oliva
plHypertrophic olivary degeneration= en
csHypertrofická olivární degeneraceHypertrofická degenerace olivy
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
MONDO975885Evalidated

E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.

3

Classification

Preferential parent (Orphanet linearisation):

Parents in the classifications (1):

No children.

4

Genes

0 direct

Orphanet records no gene directly on this code.

5

Prevalence and incidence

2 records
TypeClassValueAreaQualificationValidationSource
Cases/families158 casesWorldwideCase(s)Validated31026459[PMID]_34485912[PMID]
Point prevalence<1 / 1 000 000—WorldwideClass onlyValidated31026459[PMID]_34485912[PMID]_ORPHANET

Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.

6

HPO phenotypes

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

7

Sources for this card