raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:228418

OBSOLETE: Microcephaly-seizures-developmental delay syndrome

inactive · referred to ORPHA:1934Early infantile developmental and epileptic encephalopathy

Synonyms: OBSOLETE: MCSZ

Type
Disease
Group
Disorder
Status
inactive
Flag
Obsolete entity

This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Early infantile epileptic encephalopathy

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Microcephaly-seizures-developmental delay syndromeOBSOLETE: MCSZ
frOBSOLETE : Syndrome de microcéphalie-épilepsie-retard de développementOBSOLETE : MCSZ
deOBSOLET: Mikrozephalie-Anfälle-Entwicklungsverzögerung-SyndromOBSOLET: MCSZ
esOBSOLETO: Síndrome de microcefalia-crisis-retraso del desarrollo
itOBSOLETO: Sindrome microcefalia-epilessia-ritardo dello sviluppoOBSOLETO: MCSZ
nlOBSOLEET: Microcefalie - epileptische aanvallen - ontwikkelingsachterstandOBSOLEET: MCSZ
ptOBSOLETO: Síndrome de microcefalia-convulsões-perturbação do desenvolvimento
plNIEAKTUALNE: Maloglowie - napady drgawek - opóznienie rozwojuNIEAKTUALNE: MCSZ
csNEAKTUÁLNÍ: Syndrom mikrocefalie, záchvatů a opožděného vývoje= en
ukЗАСТАРІЛО: Синдром мікроцефалії-судом-затримки розвиткуЗАСТАРІЛО: MCSZ
zh弃用:小头-惊厥-发育迟缓综合征小头畸形伴癫痫
trEski adı: Mikrosefali-nöbet-gelişme geriliği sendromuMCSZ
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