(Q3508774)

English

Wiedemann-Rautenstrauch syndrome

very rare disorder with features of premature aging recognizable at birth, decreased subcutaneous fat, hypotrichosis, relative macrocephaly and dysmorphism

neonatal progeroid syndrome
Wiedemann-Rautenstrauch Syndrome
PROGEROID SYNDROME, NEONATAL

In more languages

Statements

developmental defect during embryogenesis

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

class of disease

0 references

progeroid syndrome

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

genetic syndromic intellectual disability

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

secondary ectropion

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

genetic lipodystrophy

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

multiple congenital anomalies/dysmorphic syndrome-intellectual disability

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

developmental anomaly of metabolic origin

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

malformation syndrome with skin/mucosae involvement

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

Hans-Rudolf Wiedemann

0 references

health specialty

0 references

genetic association

1 reference

Open Targets Platform

24 August 2023

https://platform.opentargets.org/evidence/ENSG00000148606/MONDO_0009910

based on heuristic

inferred from an Open Targets association score over 0.7

259.8

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

NCI Thesaurus ID

C121565

mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

http://www.orpha.net/ORDO/Orphanet_3455

0 references

Identifiers

MeSH descriptor ID

mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

1 reference

imported from Wikimedia project

English Wikipedia

GARD rare disease ID

0 references

1 reference

imported from Wikimedia project

English Wikipedia

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

ICD-11 (foundation)

0 references

0 references

mapping relation type

2 references

imported from Wikimedia project

English Wikipedia

Monarch Disease Ontology release 2018-06-29

28 July 2018

mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

UniProt disease ID

0 references

Sitelinks

Wikipedia(8 entries)

dewiki Wiedemann-Rautenstrauch-Syndrom
enwiki Wiedemann–Rautenstrauch syndrome
fawiki سندرم ویدمان-راوتن‌اشتراوخ
fiwiki Wiedemann–Rautenstrauchin oireyhtymä
frwiki Syndrome progéroïde néonatal
plwiki Zespół Wiedemanna-Rautenstraucha
ruwiki Синдром Видемана — Раутенштрауха
simplewiki Neonatal progeroid syndrome

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

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