Progressive spasticity

Symptom Information:

Symptom ID: HPO:0002191
Synonyms:
Spasticity, progressive [HPO:0002191]
Progressive spasticity [OMIM:Progressive spasticity]
Spasticity, progressive [OMIM:Spasticity, progressive]
Quality:
Cross references:
OMIM: "Progressive spasticity" [OMIM:Progressive spasticity]
OMIM: "Spasticity, progressive" [OMIM:Spasticity, progressive]
Is a (Direct Parents):
HPO         Spasticity
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the nervous system(HPO:0000707)
          Abnormality of nervous system physiology(HPO:0012638)
             Abnormality of central motor function(HPO:0011442)
                Abnormal pyramidal signs(HPO:0007256)
                   Hypertonia(HPO:0001276)
                      Spasticity(HPO:0001257)
                         Progressive spasticity(HPO:0002191)
MedDRA:
Database Frequency: 12 / 7739
Resource:

All diseases associated with this symptom:

Autosomal dominant spastic paraplegia type 13 (Orphanet:100994)
Autosomal dominant spastic paraplegia type 4 (Orphanet:100985)
Autosomal dominant spastic paraplegia type 6 (Orphanet:100988)
Autosomal recessive spastic paraplegia type 14 (Orphanet:100995)
Behr syndrome (Orphanet:1239)
GTP cyclohydrolase I deficiency (Orphanet:2102)
KRABBE DISEASE (OMIM:245200)
Krabbe disease (Orphanet:487)
LUBS X-LINKED MENTAL RETARDATION SYNDROME (OMIM:300260)
Pelizaeus-Merzbacher-like due to GJC2 mutation (Orphanet:280282)
Pelizaeus-Merzbacher-like due to HSPD1 mutation (Orphanet:280288)
Pontocerebellar hypoplasia, type 9 (OMIM:615809)