Abnormal myelination
Symptom Information:
Symptom ID: | HPO:0012447 | ||
Synonyms: |
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Quality: | |||
Cross references: |
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Is a (Whole tree): |
HPO:
MedDRA: |
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Database Frequency: | 7 / 7739 | ||
Resource: |
All diseases associated with this symptom:
14q11.2 microdeletion syndrome | (Orphanet:261120) |
Autosomal recessive spastic paraplegia type 45 | (Orphanet:320396) |
Congenital cataract-hypertrophic cardiomyopathy-mitochondrial myopathy syndrome | (Orphanet:1369) |
Congenital muscular dystrophy type 1A | (Orphanet:258) |
Maternal hyperphenylalaninemia | (Orphanet:2209) |
Monosomy 18q | (Orphanet:1600) |
Xeroderma pigmentosum complementation group B | (Orphanet:276252) |