raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:431

Ichthyosis-male hypogonadism syndrome

inactive · moved to ORPHA:1643Xp22.3 microdeletion syndrome

Type
Disease
Group
Disorder
Status
inactive
Flag
Deprecated entity

This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Xp22.3 microdeletion syndrome

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enIchthyosis-male hypogonadism syndrome
frSyndrome d'hypogonadisme congénital-ichtyose
deIchthyose und männlicher Hypogonadismus
esSíndrome de ictiosis-hipogonadismo masculino
itIpogonadismo congenito con ittiosi
nlIchthyosis - mannelijk hypogonadisme-syndroom
ptSíndrome de ictiose-hipogonadismo masculino
plRybia łuska - hipogonadyzm męski
csSyndrom zahrnující ichtyózu a mužský hypogonadismus
ukСиндром іхтіозу - чоловічого гіпогонадизму
zh鱼鳞病-男性性腺功能减退综合征
trİktiyoz-erkek hipogonadizm sendromu
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
OMIM308200Evalidated
MeSHC537365Evalidated

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

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