Spastic diplegia
Symptom Information:
Symptom ID: | HPO:0001264 | ||||
Synonyms: |
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Quality: | |||||
Cross references: |
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Is a (Direct Parents): |
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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 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) |
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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) |