Morphological abnormality of the central nervous system

Symptom Information:

Symptom ID: HPO:0002011
Synonyms:
Central nervous system disease [HPO:0002011]
Quality:
Cross references:
Is a (Direct Parents):
HPO         Abnormality of the subarachnoid space
HPO         Abnormality of nervous system morphology
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:
Database Frequency: 5 / 7739
Resource:

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)