raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:1981

Fanconi syndrome-ichthyosis-dysmorphism syndrome

inactive · moved to ORPHA:2697Arthrogryposis-renal dysfunction-cholestasis syndrome

Synonyms: Deal-Barrat-Dillon syndrome

Type
Disease
Group
Disorder
Status
inactive
Flag
Deprecated entity

This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Arthrogryposis-renal dysfunction-cholestasis syndrome

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enFanconi syndrome-ichthyosis-dysmorphism syndromeDeal-Barrat-Dillon syndrome
frSyndrome de Fanconi-ichtyose-dysmorphieSyndrome de Deal-Barratt-Dillon
deFanconi-Syndrom-Ichthyose-Dysmorphie-SyndromDeal-Barratt-Dillon-Syndrom
esSíndrome de Fanconi-ictiosis-dismorfiaSíndrome de Deal-Barratt-Dillon
itSindrome di Fanconi - ittiosi - dismorfismiSindrome di Deal-Barratt-Dillon
nlSyndroom van Fanconi - ichthyosis - dysmorfie-syndroomSyndroom van Deal-Barrat-Dillon
ptSíndrome de ictiose-síndrome de Fanconi-dismorfiaSíndrome Deal-Barratt-Dillon
plZespół Fanconiego - rybia łuska - dysmorfizmZespół Deala, Barrata i Dillona
csSyndrom zahrnující Fanconiho syndrom, ichtyózu a dysmorfismusDealův-Barratův-Dillonův syndrom · Deal-Barrat-Dillonův syndrom
ukСиндром Фанконі-іхтіоз-дизморфізмСиндром Діла-Баррата-Діллона
zh范可尼综合征-鱼鳞病-畸形综合征Deal-Barrat-Dillon综合征
trFanconi sendromu-iktiyozis-dismorfizm sendromuDeal-Barrat-Dillon sendromu
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