Psychomotor deterioration
Symptom Information:
Symptom ID: | HPO:0002361 | ||||||||||||||||||||||
Synonyms: |
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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) Psychomotor deterioration(HPO:0002361) MedDRA: Nervous system disorders(MedDRA:10029205) Mental impairment disorders(MedDRA:10057167) Psychomotor deterioration(HPO:0002361) Mental deterioration(HPO:0001268) Psychomotor deterioration(HPO:0002361) |
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Database Frequency: | 26 / 7739 | ||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
Aceruloplasminemia | (Orphanet:48818) |
Adult polyglucosan body disease | (Orphanet:206583) |
Atherosclerosis - deafness - diabetes - epilepsy - nephropathy | (Orphanet:1192) |
CADASIL | (Orphanet:136) |
CLN1 disease | (Orphanet:228329) |
CLN3 disease | (Orphanet:228346) |
CLN9 disease | (Orphanet:228357) |
Cerebroretinal vasculopathy | (Orphanet:3421) |
Combined oxidative phosphorylation deficiency type 23 | (ORPHA:444013) |
Gaucher disease | (Orphanet:355) |
Gaucher disease type 3 | (Orphanet:77261) |
HERNS syndrome | (Orphanet:63261) |
Hereditary vascular retinopathy | (Orphanet:71291) |
Huntington disease | (Orphanet:399) |
Hyperammonemia due to N-acetylglutamate synthetase deficiency | (Orphanet:927) |
Joubert syndrome 5 | (OMIM:610188) |
Leigh syndrome with leukodystrophy | (Orphanet:255241) |
MEGDEL syndrome | (Orphanet:352328) |
MELAS | (Orphanet:550) |
Menkes disease | (Orphanet:565) |
Microcephaly-capillary malformation syndrome | (Orphanet:294016) |
Niemann-Pick disease type C | (Orphanet:646) |
PELIZAEUS-MERZBACHER DISEASE | (OMIM:312080) |
Retinal vasculopathy and cerebral leukodystrophy | (Orphanet:247691) |
Tay-Sachs disease | (Orphanet:845) |
Wolfram syndrome | (Orphanet:3463) |