raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:97336

Panner disease

Synonyms: Aseptic necrosis of the capital humerus · Osteochondrosis of the capital humerus

Type
Disease
Group
Disorder
Inheritance
Not applicable
Age of onset
Childhood
Status
active

A rare osteochondrosis of the capitellum of the humerus, characterized by involvement of the dominant upper limb and onset before the age of 10 years. It results from lateral compression injuries of the elbow typically occurring in children practising sports such as baseball and throw. It should be distinguished from osteochondritis dissecans of the capitellum, occurring later, in adolescents.

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Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enPanner diseaseAseptic necrosis of the capital humerus · Osteochondrosis of the capital humerus
frMaladie de PannerNécrose aseptique des condyles huméraux · Ostéochondrite des condyles huméraux
dePanner-KrankheitAseptische Nekrose des Capitulum humeri · Osteochondrose des Capitulum humeri
esEnfermedad de PannerNecrosis aséptica de la cabeza del húmero · Necrosis aséptica del capítulo del húmero · Osteocondrosis de la cabeza del húmero · Osteocondrosis del capítulo del húmero
itMalattia di PannerNecrosi asettica dei condili omerali · Osteocondrosi dei condili omerali
nlZiekte van PannerAseptische necrose van de humeruskop · Osteochondrose van de humeruskop
ptDoença de Panner
plChoroba PanneraJałowa martwica głowy kości ramiennej · Osteochondroza głowy kości ramiennej
csPannerova nemocAseptická nekróza hlavice humeru · Osteochondróza hlavice humeru
ukХвороба ПаннераАсептичний некроз великогомілкової кістки · Остеохондроз головки плечової кістки
zhPanner病肱骨小头无菌性坏死
trPanner hastalığıBaş humerusun osteokondrozu · Baş humerusun aseptik nekrozu

Definition in:

2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
ICD-10M92.0NTBTinclusionvalidated
ICD-11FB82.1NTBTindexvalidated
MONDO0019969Evalidated
UMLSC4759831Evalidated

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

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Classification

Preferential parent (Orphanet linearisation):

Parents in the classifications (1):

No children.

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Genes

0 direct

Orphanet records no gene directly on this code.

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Prevalence and incidence

1 record
TypeClassValueAreaQualificationValidationSource
Point prevalenceUnknown—WorldwideClass onlyNot yet validatedORPHANET

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

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HPO phenotypes

11 annotations · validated 2019-06-14
HPOTerm (as annotated by Orphanet)Diagnostic
Very frequent (99-80%)
HP:0009810Abnormality of upper limb joint
HP:0040188Osteochondrosis
Frequent (79-30%)
HP:0031095Abnormal humerus morphology
HP:0030835Elbow pain
HP:0001386Joint swelling
HP:0001377Limited elbow extension
HP:0002996Limited elbow movement
Occasional (29-5%)
HP:0001871Abnormality of blood and blood-forming tissues
HP:0003945Irregular articular surfaces of the elbow joints
HP:0030865Large elbow
HP:0025259Stiff elbow

Run the differential on the 2 obligate / very frequent terms

Annotation source: 30483677[PMID]_25663360[PMID]

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Sources for this card