raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:2739

Onycho-tricho-dysplasia-neutropenia syndrome

inactive · moved to ORPHA:33364Trichothiodystrophy

Synonyms: Itin syndrome · ONMR syndrome · Trichothiodystrophy type G

Type
Disease
Group
Disorder
Status
inactive
Flag
Deprecated entity

This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Trichothiodystrophy

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOnycho-tricho-dysplasia-neutropenia syndromeItin syndrome · ONMR syndrome · Trichothiodystrophy type G
frSyndrome d'onycho-tricho-dysplasie-neutropénieSyndrome ONMR · Syndrome d'Itin · Trichothiodystrophie type G
deOnycho-Tricho-Dysplasie - NeutropenieItin-Syndrom · ONMR-Syndrom · Trichothiodystrophie Typ G
esSíndrome de onicotricodisplasia-neutropeniaSíndrome de Itin · Tricotiodistrofia tipo G
itOnico-trico-displasia - neutropeniaSindrome di Itin · Tricotiodistrofia, tipo G
nlOnycho-tricho-dysplasie - neutropenie-syndroomONMR-syndroom · Syndroom van Itin · Trichothiodystrofie type G
ptSíndrome de onico-trico-displasia-neutropeniaSíndrome Itin · Síndrome ONMR · Tricotiodistrofia tipo G
plDysplazja paznokci i włosów z neutropeniąTrichotiodystrofia typu G · Zespół Itina · Zespół ONMR
csSyndrom zahrnující onychotrichodysplázii a neutropeniiONMR syndrom · Trichothiodystrofie, typ G · Itinův syndrom
ukСиндром оніхотриходисплазії-нейтропеніїСиндром Ітіна · Синдром ONMR · Трихотіодистрофія типу G
zh指甲-毛发-发育不良-中性粒细胞减少症综合征毛发低硫营养不良,G型
trOniko-triko-displazi-nötropeni sendromuItin sendromu · ONMR sendromu · Trikotiyodistrofi tip G
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
OMIM258360Evalidated
UMLSC1850316Evalidated

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