raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:3105

Robinow-like syndrome

inactive · moved to ORPHA:709Peters plus syndrome

Synonyms: Saal-Greenstein syndrome

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 Peters plus syndrome

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enRobinow-like syndromeSaal-Greenstein syndrome
frSyndrome Robinow-likeSyndrome de Saal-Greenstein
deRobinow-ähnliches SyndromSaal-Greenstein-Syndrom
esSíndrome similar a RobinowSíndrome de Robinow-like · Síndrome de Saal-Greenstein
itSindrome Robinow-simileSindrome di Saal-Greenstein
nlRobinow-achtig syndroomSyndroom van Saal-Greenstein
ptSíndrome Robinow-likeSíndrome Saal-Greenstein
plZespół podobny do zespołu RobinowaZespół Saala i Greensteina
csSyndrom podobný Robinowovu syndromuSaalův-Greensteinův syndrom · Saal-Greensteinův syndrom
ukСиндром Робінов-подібнийСиндром Саала-Грінштейна
zh类Robinow综合征Saal-Greenstein综合征
trRobinow-benzeri sendromSaal-Greenstein 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