ORPHA:3362

OBSOLETE: Trichomegaly-cataract-hereditary spherocytosis syndrome

Synonyms: OBSOLETE: Goldstein-Hutt syndrome

This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Familial isolated trichomegaly

Names in Orphadata languages

12 of 12 languages

Lang	Name	Synonyms
en	OBSOLETE: Trichomegaly-cataract-hereditary spherocytosis syndrome	OBSOLETE: Goldstein-Hutt syndrome
fr	OBSOLETE : Syndrome de trichomégalie-cataracte-sphérocytose	OBSOLETE : Syndrome de Goldstein-Hutt
de	OBSOLET: Trichomegalie-Katarakt-hereditäre Sphärozytose-Syndrom	OBSOLET: Goldstein-Hutt-Syndrom
es	OBSOLETO: Síndrome de tricomegalia-catarata-esferocitosis hereditaria	OBSOLETO: Síndrome de Goldstein-Hutt
it	OBSOLETO: Sindrome tricomegalia-cataratta-sferocistosi ereditaria	OBSOLETO: Sindrome di Goldstein-Hutt
nl	OBSOLEET: Trichomegalie - cataract - erfelijke sferocytose-syndroom	OBSOLEET: Syndroom van Goldstein-Hutt
pt	OBSOLETO: Síndrome de tricomegalia-catarata-esferocitose hereditária	OBSOLETO: Síndrome Goldstein-Hutt
pl	NIEAKTUALNE: Trichomegalia - zacma - sferocytoza dziedziczna	NIEAKTUALNE: Zespół Goldsteina i Hutta
cs	NEAKTUÁLNÍ: Syndrom zahrnující trichomegalii, kataraktu a dědičnou sférocytózu	= en
uk	ЗАСТАРІЛО: Синдром трихомегалії-катаракти-спадкового сфероцитозу	ЗАСТАРІЛО: Синдром Гольдштейна-Хатта
zh	弃用：睫毛粗长症-白内障-遗传性球形红细胞增多综合征	Goldstein-Hutt综合征
tr	Eski adı: Trikomegali-katarakt-kalıtsal sferositoz sendromu	Goldstein-Hutt sendromu

qualifier = Orphanet mapping relation

No cross-references in this release.

Not placed in any Orphanet classification in this release.

No children.

0 direct

Orphanet records no gene directly on this code.

0 records

No prevalence record in this release.

Orphanet has no HPO annotation for this code in this release.