Emotional lability
Symptom Information:
Symptom ID: | HPO:0000712 | |||||||||||||||||||||||||||||||
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 physiology(HPO:0012638) Abnormality of higher mental function(HPO:0011446) Behavioral abnormality(HPO:0000708) Abnormal emotion/affect behavior(HPO:0100851) Abnormal fear/anxiety-related behavior(HPO:0100852) Emotional lability(HPO:0000712) MedDRA: |
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Database Frequency: | 44 / 7739 | |||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
2q23.1 microdeletion syndrome | (Orphanet:228402) |
AMYOTROPHIC LATERAL SCLEROSIS 10 WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA | (OMIM:612069) |
ANGIOMATOSIS, DIFFUSE CORTICOMENINGEAL, OF DIVRY AND VAN BOGAERT | (OMIM:206570) |
Acrodermatitis enteropathica, zinc deficiency type | (Orphanet:37) |
Alexander disease | (Orphanet:58) |
Aromatic L-amino acid decarboxylase deficiency | (Orphanet:35708) |
Autosomal recessive progressive external ophthalmoplegia | (Orphanet:254886) |
Autosomal recessive spastic ataxia - optic atrophy - dysarthria | (Orphanet:254343) |
Autosomal recessive spastic paraplegia type 20 | (Orphanet:101000) |
Autosomal recessive spastic paraplegia type 26 | (Orphanet:101006) |
Bardet-Biedl syndrome 2 | (OMIM:615981) |
Bardet-Biedl syndrome 7 | (OMIM:615984) |
CACH syndrome | (Orphanet:135) |
CARASIL | (Orphanet:199354) |
CATARACT, CONGENITAL, WITH MENTAL IMPAIRMENT AND DENTATE GYRUS ATROPHY | (OMIM:607674) |
CLN13 disease | (Orphanet:352709) |
COGNITIVE IMPAIRMENT WITH OR WITHOUT CEREBELLAR ATAXIA | (OMIM:614306) |
Carbamoylphosphate synthetase deficiency | (Orphanet:147) |
Congenital or early infantile CACH syndrome | (Orphanet:157713) |
Cree leukoencephalopathy | (Orphanet:99854) |
Familial dysautonomia | (Orphanet:1764) |
Gerstmann-Straussler-Scheinker syndrome | (Orphanet:356) |
Glycogen storage disease due to phosphoglycerate kinase 1 deficiency | (Orphanet:713) |
Hartnup syndrome | (Orphanet:2116) |
Hereditary sensory and autonomic neuropathy type 4 | (Orphanet:642) |
Hypertryptophanemia | (Orphanet:2224) |
Infantile-onset ascending hereditary spastic paralysis | (Orphanet:293168) |
Isolated CoQ-cytochrome C reductase deficiency | (Orphanet:1460) |
Juvenile amyotrophic lateral sclerosis | (Orphanet:300605) |
Juvenile or adult CACH syndrome | (Orphanet:157719) |
Juvenile primary lateral sclerosis | (Orphanet:247604) |
LUJAN-FRYNS SYNDROME | (OMIM:309520) |
Late infantile CACH syndrome | (Orphanet:157716) |
METACHROMATIC LEUKODYSTROPHY | (OMIM:250100) |
MULTIPLE SCLEROSIS, SUSCEPTIBILITY TO | (OMIM:126200) |
McLeod neuroacanthocytosis syndrome | (Orphanet:59306) |
NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2B | (OMIM:610217) |
Neurodegeneration with brain iron accumulation due to C19orf12 mutation | (Orphanet:289560) |
Neuroferritinopathy | (Orphanet:157846) |
Ovarioleukodystrophy | (Orphanet:99853) |
PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 4 | (OMIM:615830) |
Rapid-onset dystonia-parkinsonism | (Orphanet:71517) |
Sporadic Leigh syndrome | (Orphanet:255199) |
Wilson-Turner syndrome | (Orphanet:3459) |