(Q55785058)

English

retinitis pigmentosa and Erythrocytic Microcytosis; RPEM

human disease

Retinitis Pigmentosa and Erythrocytic Microcytosis
RPEM

In more languages

edit

Statements

0 references

1 reference

Hypomorphic mutations in TRNT1 cause retinitis pigmentosa with erythrocytic microcytosis.

subclass of

genetic disease

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

28 July 2018

2 references

Hypomorphic mutations in TRNT1 cause retinitis pigmentosa with erythrocytic microcytosis.

stated in

Open Targets Platform

retrieved

24 August 2023

reference URL

https://platform.opentargets.org/evidence/ENSG00000072756/MONDO_0014850

based on heuristic

inferred from an Open Targets association score over 0.7

Identifiers

0 references

mapping relation type

exact match

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

28 July 2018

mapping relation type

exact match

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

28 July 2018

0 references

(Q55785058)

retinitis pigmentosa and Erythrocytic Microcytosis; RPEM

Statements

Identifiers

Sitelinks

Wikipedia(0 entries)

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)