Pseudobulbar signs
Symptom Information:
Symptom ID: | HPO:0002200 | ||||||||||||||||||||||||||||||||
Synonyms: |
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Quality: | |||||||||||||||||||||||||||||||||
Cross references: |
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Is a (Direct Parents): | |||||||||||||||||||||||||||||||||
Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the nervous system(HPO:0000707) Abnormality of nervous system morphology(HPO:0012639) Morphological abnormality of the central nervous system(HPO:0002011) Pseudobulbar signs(HPO:0002200) MedDRA: |
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Database Frequency: | 15 / 7739 | ||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
AMYOTROPHIC LATERAL SCLEROSIS 2, JUVENILE | (OMIM:205100) |
ANGIOMATOSIS, DIFFUSE CORTICOMENINGEAL, OF DIVRY AND VAN BOGAERT | (OMIM:206570) |
Autosomal recessive spastic ataxia - optic atrophy - dysarthria | (Orphanet:254343) |
Autosomal recessive spastic paraplegia type 15 | (Orphanet:100996) |
Autosomal recessive spastic paraplegia type 20 | (Orphanet:101000) |
Autosomal recessive spastic paraplegia type 46 | (Orphanet:320391) |
CARASIL | (Orphanet:199354) |
COGNITIVE IMPAIRMENT WITH OR WITHOUT CEREBELLAR ATAXIA | (OMIM:614306) |
Juvenile primary lateral sclerosis | (Orphanet:247604) |
Neurodegeneration with brain iron accumulation due to C19orf12 mutation | (Orphanet:289560) |
SPASTIC PARAPLEGIA 50, AUTOSOMAL RECESSIVE | (OMIM:612936) |
Severe intellectual deficit and progressive spastic paraplegia | (Orphanet:280763) |
Sporadic Leigh syndrome | (Orphanet:255199) |
Wilson disease | (Orphanet:905) |
Wilson-Turner syndrome | (Orphanet:3459) |