ORPHA:1420

OBSOLETE: Lethal chondrodysplasia, Moerman type

Synonyms: OBSOLETE: Moerman-Vandenberghe-Fryns syndrome

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

Names in Orphadata languages

12 of 12 languages

Lang	Name	Synonyms
en	OBSOLETE: Lethal chondrodysplasia, Moerman type	OBSOLETE: Moerman-Vandenberghe-Fryns syndrome
fr	OBSOLETE : Chondrodysplasie létale type Moerman	OBSOLETE : Syndrome de Moerman-Vandenberghe-Fryns
de	OBSOLET: Chondrodysplasie, letale, Typ Moerman	OBSOLET: Moerman-Vandenberghe-Fryns-Syndrom
es	OBSOLETO: Condrodisplasia letal tipo Moerman	OBSOLETO: Síndrome de Moerman-Vandenberghe-Fryns
it	OBSOLETO: Condrodisplasia letale, tipo Moerman	OBSOLETO: Sindrome di Moerman-Van den Berghe-Fryns
nl	OBSOLEET: Letale chondrodysplasie, Moerman-type	OBSOLEET: Moerman-Vandenberghe-Frynssyndroom
pt	OBSOLETO: Condrodisplasia letal, tipo Moerman	OBSOLETO: Síndrome Moerman-Vandenberghe-Fryns
pl	NIEAKTUALNE: Smiertelna chondrodysplazja typu Moermana	NIEAKTUALNE: Zespół Moermana, Vandenberghe i Frynsa
cs	NEAKTUÁLNÍ: Letální chondrodysplázie, Moermanův typ	NEAKTUÁLNÍ: Moermanův-Vandenbergheův-Frynsův syndrom · NEAKTUÁLNÍ: Moerman-Vandenbergh-Frynsův syndrom
uk	ЗАСТАРІЛО: Летальна хондродисплазія, тип Моермана	ЗАСТАРІЛО: Синдром Мурмана-Ванденберге-Фринса
zh	弃用：致命性软骨发育不良Moerman型	Moerman-Vandenberghe-Fryns综合征
tr	Eski adı: Letal kondrodisplazi, Moerman tipi	Moerman-Vandenberghe-Fryns 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.