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Leukodystrophy, Hypomyelinating, 19, Transient Infantile (HLD19)

Alias:
Hld19
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Leukodystrophy, Hypomyelinating, 19, Transient Infantile, also known as hld19, is related to hypomyelinating leukodystrophy 19. An important gene associated with Leukodystrophy, Hypomyelinating, 19, Transient Infantile is TMEM63A (Transmembrane Protein 63A). Affiliated tissues include brain and spinal cord, and related phenotypes are delayed cns myelination and pendular nystagmus
Related ID：
MALACARDS：LKD032
OMIM：618688
MESH：D020279

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Unknown
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1
5
2
LKD032

Medical Symptom

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Description
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HPO Source Accession
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Gene & Mutation

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No data available

Disease Model

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Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

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