Morphological abnormality of the central nervous system
Symptom Information:
Symptom ID: | HPO:0002011 | ||||
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the nervous system(HPO:0000707) Abnormality of nervous system morphology(HPO:0012639) Morphological abnormality of the central nervous system(HPO:0002011) MedDRA: |
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Database Frequency: | 5 / 7739 | ||||
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All diseases associated with this symptom:
Arthrogryposis - renal dysfunction - cholestasis | (Orphanet:2697) |
Blau syndrome | (Orphanet:90340) |
Hypocomplementemic urticarial vasculitis | (Orphanet:36412) |
Riboflavin transporter deficiency | (Orphanet:97229) |
Sialidosis type 1 | (Orphanet:812) |