Neuronal loss in central nervous system

Symptom Information:

Symptom ID: HPO:0002529
Synonyms:
Neuronal loss [HPO:0002529]
Neuronal loss [OMIM:Neuronal loss]
Quality:
Cross references:
OMIM: "Neuronal loss" [OMIM:Neuronal loss]
Is a (Direct Parents):
HPO         Atrophy/Degeneration affecting the central nervous system
Is a (Whole tree): HPO:
MedDRA:
Database Frequency: 37 / 7739
Resource:

All diseases associated with this symptom:

AMYOTROPHIC LATERAL SCLEROSIS 6, WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA (OMIM:608030)
AMYOTROPHIC LATERAL SCLEROSIS 8 (OMIM:608627)
Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia (Orphanet:313808)
Alpers syndrome (Orphanet:726)
Behavioral variant of frontotemporal dementia (Orphanet:275864)
Christianson syndrome (Orphanet:85278)
Classical progressive supranuclear palsy (Orphanet:240071)
Congenital neuronal ceroid lipofuscinosis (Orphanet:168486)
ENCEPHALOPATHY, PROGRESSIVE, WITH OR WITHOUT LIPODYSTROPHY (OMIM:615924)
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 14 (OMIM:614959)
Encephalopathy due to prosaposin deficiency (Orphanet:139406)
FRONTOTEMPORAL DEMENTIA (OMIM:600274)
FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 1 (OMIM:105550)
Familial encephalopathy with neuroserpin inclusion bodies (Orphanet:85110)
Fatal familial insomnia (Orphanet:466)
Fatal infantile cytochrome C oxidase deficiency (Orphanet:1561)
Frontotemporal dementia (Orphanet:282)
Frontotemporal dementia with motor neuron disease (Orphanet:275872)
Huntington disease (Orphanet:399)
Infantile neuroaxonal dystrophy (Orphanet:35069)
Juvenile Huntington disease (Orphanet:248111)
Lissencephaly type 3 - metacarpal bone dysplasia (Orphanet:86822)
McLeod neuroacanthocytosis syndrome (Orphanet:59306)
Multiple congenital anomalies-hypotonia-seizures syndrome type 2 (Orphanet:300496)
NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2A (OMIM:256600)
NIEMANN-PICK DISEASE, TYPE C1 (OMIM:257220)
PARKINSON DISEASE, LATE-ONSET (OMIM:168600)
PEHO syndrome (Orphanet:2836)
PICK DISEASE OF BRAIN (OMIM:172700)
Progressive non-fluent aphasia (Orphanet:100070)
RIGIDITY AND MULTIFOCAL SEIZURE SYNDROME, LETHAL NEONATAL (OMIM:614498)
Recessive mitochondrial ataxia syndrome (Orphanet:94125)
SKELETAL DYSPLASIA AND PROGRESSIVE CENTRAL NERVOUS SYSTEM DEGENERATION,LETHAL (OMIM:602613)
SUPRANUCLEAR PALSY, PROGRESSIVE, 2 (OMIM:609454)
Spinocerebellar ataxia type 17 (Orphanet:98759)
Spinocerebellar ataxia type 23 (Orphanet:101108)
X-linked spinocerebellar ataxia type 3 (Orphanet:85297)