(Q50846110)

English

HSD10 disease

No description defined

2-methyl-3-hydroxybutyric aciduria. 2-methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency
MHBD deficiency
HSD10 deficiency

In more languages

default for all languages

No label defined

No description defined

Statements

class of disease

0 references

X-linked intellectual disability

0 references

genetic association

1 reference

Open Targets Platform

24 August 2023

https://platform.opentargets.org/evidence/ENSG00000072506/Orphanet_391417

based on heuristic

inferred from an Open Targets association score over 0.7

Identifiers

0 references

GARD rare disease ID

0 references

Genetics Home Reference Conditions ID

0 references

0 references

0 references

1 reference

based on heuristic

inferred by common Orphanet mappings on source and on Wikidata

16 June 2023

Sitelinks

Wikipedia(1 entry)

dewiki HSD10-Mangel

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)

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