raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:775

OBSOLETE: X-linked intellectual disability, Martinez type

inactive · referred to ORPHA:777X-linked non-syndromic intellectual disability

Type
Malformation syndrome
Group
Disorder
Status
inactive
Flag
Obsolete entity

This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using X-linked non-syndromic intellectual disability

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: X-linked intellectual disability, Martinez type
frOBSOLETE : Déficience intellectuelle liée à l'X type Martinez
deOBSOLET: Intelligenzminderung, X-chromosomale, Typ Martinez
esOBSOLETO: Discapacidad intelectual ligada al cromosoma X tipo Martinez
itOBSOLETO: Ritardo mentale legato all'X, tipo Martinez
nlOBSOLEET: Intellectuele achterstand, X-gebonden, Martinez-type
ptOBSOLETO: Perturbação do desenvolvimento intelectual ligada ao X, tipo Martinez
plNIEAKTUALNE: Niepelnosprawnosc intelektualna sprzezona z chromosomem X typu Martineza
csNEAKTUÁLNÍ: X-vázaná mentální retardace, Martinezův typ
ukЗАСТАРІЛО: Х-зчеплена розумова відсталість, тип Мартінеса
zh弃用:X连锁智力障碍,Martinez亚型
trEski adı: X'e bağlı zihinsel yetersizlik, Martinez tipi
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