hypomyelinating leukodystrophy 10

Human disease

Facts

4 properties
Instance of
rare disease, class of disease[2]
Subclass of
hypomyelinating leukodystrophy, autosomal recessive disease[3][4]
Genetic association
PYCR2[5]
On focus list of Wikimedia project
WikiProject Medicine[6]
🏷️ Also known as
en HLD10 en hypomyelinating leukodystrophy 10 en hypomyelinating leukodystrophy type 10 en LEUKODYSTROPHY, HYPOMYELINATING, 10 en LEUKODYSTROPHY, HYPOMYELINATING, 10; HLD10 en Leukodystrophy, Hypomyelinating, type 10
🔖 Identifiers · 6
Disease Ontology ID
DOID:0060788
OMIM ID
616420
UMLS CUI
C4225332
UniProt disease ID
DI-04450

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Summary

hypomyelinating leukodystrophy 10 is a rare disease[1].

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Use these citations when quoting this entity in research, articles, AI prompts, or wherever provenance matters. We aggregate Wikidata + Wikipedia + authoritative open-data sources; the stitched, scored, cross-referenced view is what 4ort.xyz contributes.

APA 4ort.xyz Knowledge Graph. (2026). hypomyelinating leukodystrophy 10. Retrieved May 3, 2026, from https://4ort.xyz/entity/hypomyelinating-leukodystrophy-10
MLA “hypomyelinating leukodystrophy 10.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/hypomyelinating-leukodystrophy-10.
BibTeX @misc{4ortxyz_hypomyelinating-leukodystrophy-10_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{hypomyelinating leukodystrophy 10}}, year = {2026}, url = {https://4ort.xyz/entity/hypomyelinating-leukodystrophy-10}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): hypomyelinating leukodystrophy 10 — https://4ort.xyz/entity/hypomyelinating-leukodystrophy-10 (retrieved 2026-05-03)

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