Emotional lability

Symptom Information:

Symptom ID: HPO:0000712
Synonyms:
Emotional instability [HPO:0000712]
Pseudobulbar affect [Orphanet:43090]
Mood swings (finding) [Orphanet:43090]
Pseudobulbar affect (finding) [Orphanet:43090]
Mood swings [Orphanet:43090]
Emotional instability [OMIM:Emotional instability]
Emotional lability [OMIM:Emotional lability]
Pseudobulbar signs/spasmodic laugh and cry [Orphanet:43090]
Mood altered [Orphanet:43090]
Mood swings [MedDRA:10027951]
Mood variable [MedDRA:10027951]
Mood altered [MedDRA:10027940]
Affect altered [MedDRA:10027940]
Altered mood [MedDRA:10027940]
Bad mood [MedDRA:10027940]
Mood alteration NOS [MedDRA:10027940]
Mood change [MedDRA:10027940]
Affect alteration [MedDRA:10027940]
Affect lability [MedDRA:10054196]
Emotional instability [MedDRA:10054196]
Emotional lability [MedDRA:10054196]
Instability emotional [MedDRA:10054196]
Labile affect [MedDRA:10054196]
Lability emotional [MedDRA:10054196]
Mental lability symptom [MedDRA:10054196]
Emotional incontinence [MedDRA:10054196]
Affective incontinence [MedDRA:10054196]
Pseudobulbar affect [MedDRA:10054196]
Emotional lability (2 patients) [OMIM:Emotional lability (2 patients)]
Emotional lability (in some) [OMIM:Emotional lability (in some)]
Emotional lability (variable) [OMIM:Emotional lability (variable)]
Quality:
Cross references:
HPO:0002200 "Pseudobulbar signs" [Orphanet:43090]
Orphanet:43090 "Pseudobulbar signs/spasmodic laugh and cry" [Orphanet:43090]
OMIM: "Emotional instability" [OMIM:Emotional instability]
OMIM: "Emotional lability" [OMIM:Emotional lability]
OMIM: "Emotional lability (2 patients)" [OMIM:Emotional lability (2 patients)]
OMIM: "Emotional lability (in some)" [OMIM:Emotional lability (in some)]
OMIM: "Emotional lability (variable)" [OMIM:Emotional lability (variable)]
UMLS:C0085633 "Mood swings" [Orphanet:43090]
UMLS:C2316460 "Pseudobulbar affect" [Orphanet:43090]
Is a (Direct Parents):
MedDRA Affect alterations NEC
MedDRA Emotional and mood disturbances NEC
Orphanet Functional anomalies of the nervous system
HPO         Abnormal fear/anxiety-related behavior
MedDRA Fluctuating mood symptoms
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:
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)