(Q6967220)

multiple congenital anomalies/dysmorphic syndrome without intellectual disability

28 July 2018

0 references

0 references

1 reference

rare genetic developmental defect during embryogenesis

28 July 2018

Mondo ID

MONDO_0009720

1 reference

X-linked recessive disease

28 July 2018

Mondo ID

MONDO_0009720

1 reference

30 November 2020

1 reference

30 November 2020

0 references

1 reference

Open Targets Platform

https://platform.opentargets.org/evidence/ENSG00000076716/MONDO_0009720

24 August 2023

reference URL

based on heuristic

inferred from an Open Targets association score over 0.7

NCI Thesaurus ID

C186306

0 references

http://www.orpha.net/ORDO/Orphanet_2662

0 references

http://purl.obolibrary.org/obo/DOID_0111842

1 reference

30 November 2020

http://identifiers.org/doid/DOID:0111842

1 reference

https://registry.identifiers.org/registry/doid

Identifiers.org

reference URL

Identifiers

MeSH descriptor ID

C538337

subject named as

Nasodigitoacoustic syndrome

1 reference

imported from Wikimedia project

28 July 2018

0 references

1 reference

30 November 2020

0 references

1 reference

1 reference

imported from Wikimedia project

28 July 2018

1 reference

English Wikipedia

KBpedia ID

NasodigitoacousticSyndrome

1 reference

KBpedia

Medical Dictionary for Regulatory Activities ID

9 July 2020

10010356

1 reference

reference URL

https://cdn.who.int/media/docs/default-source/classification/icd/icd-10/icd-10-to-meddra-map---june-2023---codes-mapping.xlsx

based on heuristic

inferred by common ICD-10 mappings on Wikidata and on source

Microsoft Academic ID

0 references

0 references

imported from Wikimedia project

2 references

English Wikipedia

28 July 2018

1 reference

28 July 2018

1 reference