Inability to walk

Symptom Information:

Symptom ID: HPO:0002540
Synonyms:
Non-ambulatory [HPO:0002540]
Abasia [OMIM:Abasia]
Inability to walk [OMIM:Inability to walk]
Abasia [MedDRA:10049460]
Quality:
Cross references:
OMIM: "Abasia" [OMIM:Abasia]
OMIM: "Inability to walk" [OMIM:Inability to walk]
Is a (Direct Parents):
MedDRA Neurological signs and symptoms NEC
HPO         Gait disturbance
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 movement(HPO:0100022)
                Gait disturbance(HPO:0001288)
                   Inability to walk(HPO:0002540)
MedDRA:
Nervous system disorders(MedDRA:10029205)
    Neurological disorders NEC(MedDRA:10029305)
       Neurological signs and symptoms NEC(MedDRA:10029306)
          Inability to walk(HPO:0002540)
Database Frequency: 19 / 7739
Resource:

All diseases associated with this symptom:

14q11.2 microdeletion syndrome (Orphanet:261120)
5q14.3 microdeletion syndrome (Orphanet:228384)
ATONIC-ASTATIC SYNDROME OF FOERSTER (OMIM:209100)
Adenylosuccinate lyase deficiency (Orphanet:46)
Allan-Herndon-Dudley syndrome (Orphanet:59)
Atypical Rett syndrome (Orphanet:3095)
Biotin-responsive basal ganglia disease (Orphanet:65284)
CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME4 (OMIM:615268)
HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 4 (OMIM:615716)
Hurler syndrome (Orphanet:93473)
MENTAL RETARDATION, AUTOSOMAL DOMINANT 9 (OMIM:614255)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION),TYPE B, 1 (OMIM:613155)
MYASTHENIC SYNDROME, CONGENITAL, 3A, SLOW-CHANNEL (OMIM:616321)
Mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria (Orphanet:1933)
Mitochondrial DNA depletion syndrome, myopathic form (Orphanet:254875)
Primary Fanconi syndrome (Orphanet:3337)
SPASTIC PARAPLEGIA 61, AUTOSOMAL RECESSIVE (OMIM:615685)
Salla disease (Orphanet:309334)
Thiamine-responsive encephalopathy (Orphanet:199348)