Human Gene Set: HP_CEREBRAL_HYPOMYELINATION


Standard name HP_CEREBRAL_HYPOMYELINATION
Systematic name M36930
Brief description Cerebral hypomyelination
Full description or abstract Reduced amount of myelin in the nervous system resulting from defective myelinogenesis in the white matter of the central nervous system. [https://orcid.org/0000-0002-0736-9199]
Collection C5: Ontology
      HPO: Human Phenotype Ontology
Source publication  
Exact source HP:0006808
Related gene sets  
External links https://hpo.jax.org/app/browse/term/HP:0006808
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Source species Homo sapiens
Contributed by Human Phenotype Ontology Group (The Jackson Laboratory (JAX))
Source platform or
identifier namespace		 Human_NCBI_Gene_ID
Dataset references  
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Version history 2026.1.Hs: Updated to HPO Release 2026-01-08.


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