raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:2113

Congenital hypothalamic hamartoma syndrome

inactive · moved to ORPHA:672Pallister-Hall syndrome

Synonyms: CHHS

Type
Malformation syndrome
Group
Disorder
Status
inactive
Flag
Deprecated entity

This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Pallister-Hall syndrome

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enCongenital hypothalamic hamartoma syndromeCHHS
frSyndrome congénital d'hamartome hypothalamique
deSyndrom des kongenitalen hypothalamischen Hamartoms= en
esSíndrome de hamartomas hipotalámicos congénitos
itSindrome dell'amartoma ipotalamico congenito= en
nlCongenitaal hamartoom van hypothalamus-syndroom= en
ptSíndrome de hamartoma hipotalâmico congénito= en
plHamartoma podwzgórza= en
csVrozené hamartomy hypotalamu= en
ukСиндром вродженої гіпоталамічної гамартоми= en
zh先天性下丘脑性错构瘤综合征= en
trDoğumsal hipotalamik hamartom sendromu= en
2

Cross-references

qualifier = Orphanet mapping relation

No cross-references in this release.

3

Classification

Not placed in any Orphanet classification in this release.

No children.

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