Progressive neurologic deterioration
Symptom Information:
Symptom ID: | HPO:0002344 | ||||||||||
Synonyms: |
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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 higher mental function(HPO:0011446) Cognitive impairment(HPO:0100543) Mental deterioration(HPO:0001268) Progressive neurologic deterioration(HPO:0002344) MedDRA: |
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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) |