(Q4653653)

English

AREDYLD syndrome

medical condition

Acrorenal defect-ectodermal dysplasia-diabetes syndrome
Acrorenal Field Defect, Ectodermal Dysplasia, and Lipoatrophic Diabetes
AREDYLD

In more languages

Statements

hereditary disorder

0 references

developmental defect during embryogenesis

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

class of disease

0 references

syndromic renal or urinary tract malformation

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

rare genetic diabetes mellitus

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

other rare diabetes mellitus

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

753.3

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

http://www.orpha.net/ORDO/Orphanet_1133

0 references

Identifiers

MeSH descriptor ID

mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

GARD rare disease ID

0 references

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

ICD-11 (foundation)

0 references

Microsoft Academic ID

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

Sitelinks

Wikipedia(2 entries)

dewiki AREDYLD-Syndrom
enwiki AREDYLD 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)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q4653653&oldid=2087124773"