(Q55785106)

English

Dias-Logan syndrome

human disease

DILOS
Intellectual developmental disorder with persistence of fetal hemoglobin

In more languages

Statements

0 references

1 reference

De Novo Gene Disruptions in Children on the Autistic Spectrum

genetic disease

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

Hereditary persistence of fetal hemoglobin

0 references

genetic association

4 references

BCL11A Haploinsufficiency Causes an Intellectual Disability Syndrome and Dysregulates Transcription

14 September 2020

https://search.clinicalgenome.org/kb/gene-validity/9630f9a3-3f90-49c6-ae8b-6313c950b1b2--2020-09-13T17:18:07

25 January 2022

https://search.clinicalgenome.org/kb/gene-validity/CGGV:assertion_9630f9a3-3f90-49c6-ae8b-6313c950b1b2-2020-09-13T171807.228Z

Open Targets Platform

24 August 2023

https://platform.opentargets.org/evidence/ENSG00000119866/MONDO_0014914

based on heuristic

inferred from an Open Targets association score over 0.7

Identifiers

0 references

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

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Wiktionary(0 entries)

Multilingual sites(0 entries)

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