(Q9390205)

autosomal dominant disease

28 July 2018

0 references

0 references

1 reference

29 November 2020

syndrome with limb reduction defects

1 reference

EEC syndrome and related syndrome

28 July 2018

Mondo ID

MONDO_0007072

1 reference

dysostosis of genetic origin with limb anomaly as a major feature

28 July 2018

Mondo ID

MONDO_0007072

1 reference

malformation syndrome with odontal and/or periodontal component

28 July 2018

Mondo ID

MONDO_0007072

1 reference

TP63 gene mutation in ADULT syndrome

28 July 2018

1 reference

29 November 2020

3 references

13 August 2019

Open Targets Platform

https://platform.opentargets.org/evidence/ENSG00000073282/MONDO_0007072

24 August 2023

reference URL

based on heuristic

inferred from an Open Targets association score over 0.7

on focus list of Wikimedia project

WikiProject Medicine

0 references

http://purl.obolibrary.org/obo/DOID_0050601

1 reference

29 November 2020

http://identifiers.org/doid/DOID:0050601

2 references

10 July 2020

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

http://www.orpha.net/ORDO/Orphanet_978

0 references

Identifiers

MeSH descriptor ID

C538052

mapping relation type

1 reference

imported from Wikimedia project

28 July 2018

0 references

1 reference

29 November 2020

1 reference

English Wikipedia

Wikimedia import URL

https://en.wikipedia.org/w/index.php?title=Acro–dermato–ungual–lacrimal–tooth_syndrome&oldid=953845006

1 reference

28 August 2019

1 reference

28 July 2018

0 references

Microsoft Academic ID

0 references

0 references

1 reference

28 August 2019

mapping relation type

1 reference

28 July 2018

mapping relation type

1 reference