raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:3313

OBSOLETE: Intellectual disability-microcephaly-unusual facies syndrome

inactive · referred to ORPHA:102283Multiple congenital anomalies/dysmorphic syndrome-intellectual disability

Synonyms: OBSOLETE: Thiele syndrome

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 Multiple congenital anomalies/dysmorphic syndrome-intellectual disability

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Intellectual disability-microcephaly-unusual facies syndromeOBSOLETE: Thiele syndrome
frOBSOLETE : Syndrome de TheileOBSOLETE : Déficience intellectuelle-microcéphalie-faciès particulier
deOBSOLET: Intelligenzminderung-Mikrozephalie-ungewöhnliche Fazies-SyndromOBSOLET: Thiele-Syndrom
esOBSOLETO: Síndrome de discapacidad intelectual-microcefalia-facies inusualOBSOLETO: Síndrome de Thiele
itOBSOLETO: Sindrome disabilità intellettiva-microcefalia-facies caratteristicaOBSOLETO: Sindrome di Thiele
nlOBSOLEET: Intellectuele achterstand - microcefalie - ongewoon gelaat-syndroomOBSOLEET: Syndroom van Thiele
ptOBSOLETO: Síndrome de perturbação do desenvolvimento intelectual-microcefalia-face peculiarOBSOLETO: Síndrome Thiele
plNIEAKTUALNE: Niepelnosprawnosc intelektualna - maloglowie - niezwykly wyglad twarzyNIEAKTUALNE: Zespół Thiele
csNEAKTUÁLNÍ: Syndrom zahrnující mentální retardaci, mikrocefalii a neobvyklé facie= en
ukЗАСТАРІЛО: Синдром розумової відсталості-мікроцефалії-незвичайної зовнішностіЗАСТАРІЛО: Синдром Тіле
zh弃用:智力障碍-小头畸形-特殊面容综合征Thiele综合征
trEski adı: zihinsel yetersizlik-mikrosefali-alışılmadık yüz sendromuThiele sendromu
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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.

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Sources for this card