Progressive neurologic deterioration

Symptom Information:

Symptom ID: HPO:0002344
Synonyms:
Neurologic deterioration [HPO:0002344]
Neurologic deterioration, progressive [HPO:0002344]
Progressive mental deterioration [HPO:0002344]
Progressive neurodegeneration [HPO:0002344]
Neurologic deterioration [OMIM:Neurologic deterioration]
Neurologic deterioration, progressive [OMIM:Neurologic deterioration, progressive]
Progressive mental deterioration [OMIM:Progressive mental deterioration]
Progressive neurodegeneration [OMIM:Progressive neurodegeneration]
Progressive neurologic deterioration [OMIM:Progressive neurologic deterioration]
Neurodegeneration, progressive [OMIM:Neurodegeneration, progressive]
Quality:
Cross references:
OMIM: "Neurologic deterioration" [OMIM:Neurologic deterioration]
OMIM: "Neurologic deterioration, progressive" [OMIM:Neurologic deterioration, progressive]
OMIM: "Progressive mental deterioration" [OMIM:Progressive mental deterioration]
OMIM: "Progressive neurodegeneration" [OMIM:Progressive neurodegeneration]
OMIM: "Progressive neurologic deterioration" [OMIM:Progressive neurologic deterioration]
OMIM: "Neurodegeneration, progressive" [OMIM:Neurodegeneration, progressive]
Is a (Direct Parents):
HPO         Mental deterioration
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 higher mental function(HPO:0011446)
                Cognitive impairment(HPO:0100543)
                   Mental deterioration(HPO:0001268)
                      Progressive neurologic deterioration(HPO:0002344)
MedDRA:
Database Frequency: 27 / 7739
Resource:

All diseases associated with this symptom:

6-pyruvoyl-tetrahydropterin synthase deficiency (Orphanet:13)
Adrenomyeloneuropathy (Orphanet:139399)
Adult-onset autosomal dominant leukodystrophy (Orphanet:99027)
CYSTINOSIS, NEPHROPATHIC (OMIM:219800)
Dihydropteridine reductase deficiency (Orphanet:226)
Familial dementia, British type (Orphanet:97345)
Fetal Gaucher disease (Orphanet:85212)
GTP cyclohydrolase I deficiency (Orphanet:2102)
Gaucher disease type 2 (Orphanet:77260)
Gaucher disease type 3 (Orphanet:77261)
Griscelli disease type 2 (Orphanet:79477)
Hurler syndrome (Orphanet:93473)
Lafora disease (Orphanet:501)
MEGALENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS 2A (OMIM:613925)
MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 2 (OMIM:615157)
Mitochondrial DNA depletion syndrome, encephalomyopathic form with renal tubulopathy (Orphanet:255235)
Mucopolysaccharidosis type 1 (Orphanet:579)
Mucopolysaccharidosis type 2 (Orphanet:580)
Multiple sulfatase deficiency (Orphanet:585)
Niemann-Pick disease type A (Orphanet:77292)
Pyruvate dehydrogenase E3 deficiency (Orphanet:2394)
Retinopathy - anemia- central nervous system anomalies (Orphanet:3088)
Sanfilippo syndrome type B (Orphanet:79270)
Short chain 3-hydroxyacyl-CoA dehydrogenase deficiency (Orphanet:35123)
Wolfram syndrome 1 (OMIM:222300)
X-linked cerebral adrenoleukodystrophy (Orphanet:139396)
Zellweger-like syndrome without peroxisomal anomalies (Orphanet:50812)