raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:319623

OBSOLETE: X-linked mendelian susceptibility to mycobacterial diseases due to CYBB deficiency

inactive · referred to ORPHA:319605X-linked mendelian susceptibility to mycobacterial diseases

Synonyms: OBSOLETE: X-linked MSMD due to CYBB deficiency

Type
Etiological subtype
Group
Subtype of 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 mendelian susceptibility to mycobacterial diseases

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: X-linked mendelian susceptibility to mycobacterial diseases due to CYBB deficiencyOBSOLETE: X-linked MSMD due to CYBB deficiency
frOBSOLETE : Prédisposition mendélienne aux infections mycobactériennes liée à l'X par déficit en CYBBOBSOLETE : MSMD liée à l'X par déficit en CYBB
deOBSOLET: X-chromosomale Suszeptibilität für Mykobakteriosen durch CYBB-Defekt
esOBSOLETO: Susceptibilidad mendeliana a enfermedades micobacterianas ligada al cromosoma X por deficiencia de CYBBOBSOLETO: SMEM ligada al cromosoma X por deficiencia de CYBB
itOBSOLETO: Suscettibilit mendeliana a malattie micobatteriche da deficit di CYBB legata all'XOBSOLETO: MSMD legata all'X da deficit di CYBB
nlOBSOLEET: X-gebonden Mendeliaanse gevoeligheid voor mycobacteriële ziekten door CYBB-deficiëntieOBSOLEET: X-gebonden MSMD door CYBB-deficiëntie
ptOBSOLETO: Susceptibilidade mendeliana a doenças micobacterianas por deficiência de CYBB ligada ao X
plNIEAKTUALNE: Mendlowska podatność na choroby mykobakteryjne sprzężona z chromosomem X spowodowana niedoborem CYBBNIEAKTUALNE: MSMD sprzężona z chromosomem X spowodowana niedoborem CYBB
csNEAKTUÁLNÍ: X-vázaná genetická vnímavost k mykobakteriální infekci způsobená CYBB deficitemNEAKTUÁLNÍ: X-vázaná MSMD způsobená CYBB deficitem
ukХ-зчеплена менделівська схильність до мікобактеріальних захворювань внаслідок дефіциту CYBBХ-зчеплена MSMD внаслідок дефіциту CYBB
zhCYBB基因缺陷所致孟德尔X连锁遗传易感分枝杆菌病CYBB基因缺陷所致X连锁MSMD
trCYBB eksikliğine bağlı mikobakteriyel hastalıklara X'e bağlı Mendel tipi yatkınlıkCYBB eksikliğine bağlı X'e bağlı MSMD
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