raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:65798

Goodman syndrome

inactive · moved to ORPHA:65759Carpenter syndrome

Synonyms: ACPS4 · Acrocephalopolysyndactyly type 4

Type
Malformation syndrome
Group
Disorder
Status
inactive
Flag
Deprecated entity

This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Carpenter syndrome

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enGoodman syndromeACPS4 · Acrocephalopolysyndactyly type 4
frSyndrome de GoodmanACPS4 · Acro-céphalo-syndactylie type 4
deGoodman-SyndromACPS4 · Akrozephalopolysyndaktylie Typ 4
esSíndrome de GoodmanACPS 4 · Acrocefalopolisindactilia tipo 4
itSindrome di GoodmanACPS4 · Acrocefalopolisindattilia, tipo 4
nlSyndroom van GoodmanACPS 4 · Acrocefalopolysyndactylie type 4
ptSíndrome GoodmanACPS4 · Acrocefalopolissindactilia tipo 4
plZespół GoodmanaACPS4 · Akrocefalopolisyndaktylia typu 4
csGoodmanův syndromACPS4 · Akrocefalopolysyndaktylie, typ 4
ukСиндром ГудменаACPS4 · Акроцефалополісиндактилія 4 типу
zhGoodman综合征尖头多指(趾)并指(趾)畸形4型
trGoodman sendromuACPS4 · Akrosefalopolisindaktili tip 4
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
OMIM201020Evalidated
ICD-10Q87.0NTBTattributedvalidated
MONDO0008711Evalidated
UMLSC0265303Evalidated
GARD2549Evalidated

E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.

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