raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:319494

Familial nonmedullary thyroid carcinoma

Type
Clinical group
Group
Group of disorders
Status
active

A rare non-syndromic form of thyroid cancer characterized by occurrence of thyroid carcinoma (TC) as the primary feature in a familial setting.

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enFamilial nonmedullary thyroid carcinoma
frCarcinome non médullaire familial de la thyroïde
deSchilddrüsenkarzinom, nicht-medulläres, familiäre Form
esCarcinoma no medular familiar de tiroides
itCarcinoma della tiroide familiare non midollare
nlFamiliaal niet-medullair thyroïd carcinoomFamiliaal niet-medullair schildkliercarcinoom
ptCarcinoma da tiroide não-medular familiar
plRodzinny nierdzeniasty rak tarczycy
csFamiliární nemedulární karcinom štítné žlázy
ukСімейна немедулярна карцинома щитоподібної залози
zh家族性非髓样甲状腺癌
trAilesel medüller olmayan tiroid karsinomu

Definition in:

2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
MONDO0017896Evalidated
MONDO17896Evalidated
UMLSC5191836Evalidated

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 (3):

Children (2):

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