raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:36204

Intestinal lymphangiectasia

Type
Clinical group
Group
Group of disorders
Inheritance
Not applicable
Age of onset
All ages
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
enIntestinal lymphangiectasia
frLymphangiectasie intestinale
deLymphangiektasie, intestinale
esLinfangiectasia intestinal
itLinfangectasia intestinale
nlIntestinale lymfangiëctasie
ptLinfangiectasia intestinal
plLimfangiektazja jelitowa
csStřevní lymfangiektázie
ukКишкова лімфангіектазія
zh肠淋巴管扩张
trBağırsak lenfanjiektazi
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
ICD-11BD92.0Especificvalidated
MONDO0018178Evalidated
MONDO18178Evalidated
MeSHD008201Evalidated
UMLSC0024215Evalidated
GARD12331Evalidated
MedDRA10025213Evalidated

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 (3):

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