raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:300766

Laminopathy with premature aging

Type
Category
Group
Group of disorders
Status
active

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.

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enLaminopathy with premature aging
frLaminopathie avec vieillissement prématuré
deLaminopathie mit vorzeitiger Alterung
esLaminopatía con envejecimiento prematuro
itLaminopatia con invecchiamento precoce
nlLaminopathie met vroegtijdige veroudering
ptLaminopatia com envelhecimento prematuro
plLaminopatia z przedwczesnym starzeniem
csLaminopatie s předčasným stárnutím
ukЛамінопатія з передчасним старінням
zh核纤层蛋白病伴早衰
trErken yaşlanma ile seyreden laminopati
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
UMLSC5567864Evalidated

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):

Children (4):

Codes that Orphanet moved or referred to this one:

4

Genes

0 direct

Orphanet records no gene directly on this code.

5

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.

6

HPO phenotypes

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

7

Sources for this card