Spastic diplegia

Symptom Information:

Symptom ID: HPO:0001264
Synonyms:
Spastic diplegia [OMIM:Spastic diplegia]
Spastic diplegia (1 patient) [OMIM:Spastic diplegia (1 patient)]
Spastic diplegia (in some) [OMIM:Spastic diplegia (in some)]
Spastic diplegia [MedDRA:10067130]
Quality:
Cross references:
OMIM: "Spastic diplegia" [OMIM:Spastic diplegia]
OMIM: "Spastic diplegia (1 patient)" [OMIM:Spastic diplegia (1 patient)]
OMIM: "Spastic diplegia (in some)" [OMIM:Spastic diplegia (in some)]
Is a (Direct Parents):
MedDRA Paralysis and paresis (excl cranial nerve)
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)
                         Spastic diplegia(HPO:0001264)
MedDRA:
Nervous system disorders(MedDRA:10029205)
    Abnormality of movement(HPO:0100022)
       Paralysis and paresis (excl cranial nerve)(MedDRA:10033800)
          Spastic diplegia(HPO:0001264)
Database Frequency: 24 / 7739
Resource:

All diseases associated with this symptom:

Anophthalmia/microphthalmia - esophageal atresia (Orphanet:77298)
Argininemia (Orphanet:90)
Congenital short bowel syndrome (Orphanet:2301)
ENCEPHALOMALACIA, MULTILOCULAR (OMIM:225700)
EPILEPSY, PHOTOGENIC, WITH SPASTIC DIPLEGIA AND MENTAL RETARDATION (OMIM:226800)
Fetal iodine syndrome (Orphanet:1910)
Glutaryl-CoA dehydrogenase deficiency (Orphanet:25)
Hyperlysinemia, type I (OMIM:238700)
INTESTINAL PSEUDOOBSTRUCTION, NEURONAL, CHRONIC IDIOPATHIC, X-LINKED (OMIM:300048)
Inherited congenital spastic tetraplegia (Orphanet:210141)
Intellectual deficit, X-linked, Brooks type (Orphanet:3056)
MENTAL RETARDATION, AUTOSOMAL DOMINANT 19 (OMIM:615075)
MICROPHTHALMIA, SYNDROMIC 1 (OMIM:309800)
Micro syndrome (Orphanet:2510)
OCULORENOCEREBELLAR SYNDROME (OMIM:257970)
PAINE SYNDROME (OMIM:311400)
Perrault Syndrome (Orphanet:2855)
Perrault Syndrome 1 (OMIM:233400)
Purine nucleoside phosphorylase deficiency (Orphanet:760)
Pyruvate dehydrogenase E3-binding protein deficiency (Orphanet:255182)
Saccharopinuria (Orphanet:3124)
Spastic diplegia, infantile type (Orphanet:1680)
TRICHORRHEXIS NODOSA SYNDROME (OMIM:275550)
WARBURG MICRO SYNDROME 1 (OMIM:600118)