Abnormal emotion/affect behavior

Symptom Information:

Symptom ID: HPO:0100851
Synonyms:
Abnormal emotion/affect behaviour [HPO:0100851]
Quality:
Cross references:
Is a (Direct Parents):
HPO         Emotional blunting
HPO         Behavioral abnormality
HPO         Happy demeanor
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)
MedDRA:
Database Frequency: 85 / 7739
Resource:

All diseases associated with this symptom:

15q13.3 microdeletion syndrome (Orphanet:199318)
16p11.2p12.2 microdeletion syndrome (Orphanet:261211)
17p11.2 microduplication syndrome (Orphanet:1713)
1q21.1 microdeletion syndrome (Orphanet:250989)
1q21.1 microduplication syndrome (Orphanet:250994)
22q11.2 deletion syndrome (Orphanet:567)
22q11.2 microduplication syndrome (Orphanet:1727)
2q32q33 microdeletion syndrome (Orphanet:251019)
3q29 microdeletion syndrome (Orphanet:65286)
48,XXXY syndrome (Orphanet:96263)
8p23.1 microdeletion syndrome (Orphanet:251071)
ACTH-dependent Cushing syndrome (Orphanet:99892)
ACTH-independent Cushing syndrome (Orphanet:99893)
ACTH-independent macronodular adrenal hyperplasia (Orphanet:189427)
Acromegaly (Orphanet:963)
Acute intermittent porphyria (Orphanet:79276)
Adiposis dolorosa (Orphanet:36397)
Aggressive systemic mastocytosis (Orphanet:98850)
Alexander disease (Orphanet:58)
Alpha-thalassemia - X-linked intellectual deficit syndrome (Orphanet:847)
Amish lethal microcephaly (Orphanet:99742)
Atypical teratoid tumor (Orphanet:99966)
Autosomal dominant hypocalcemia (Orphanet:428)
Babesiosis (Orphanet:108)
Beta-thalassemia (Orphanet:848)
Beta-thalassemia major (Orphanet:231214)
Caffey disease (Orphanet:1310)
Central congenital hypothyroidism (Orphanet:226298)
Central diabetes insipidus (Orphanet:178029)
Cerebrotendinous xanthomatosis (Orphanet:909)
Choreoacanthocytosis (Orphanet:2388)
Chronic hiccup (Orphanet:396)
Congenital hypothyroidism (Orphanet:442)
Cornelia de Lange syndrome (Orphanet:199)
Cushing syndrome due to ectopic ACTH secretion (Orphanet:99889)
Cutaneous mastocytosis (Orphanet:66646)
Distal 22q11.2 microdeletion syndrome (Orphanet:261330)
Distal 7q11.23 microdeletion syndrome (Orphanet:254351)
Ehlers-Danlos syndrome, hypermobility type (Orphanet:285)
Fabry disease (Orphanet:324)
Familial advanced sleep-phase syndrome (Orphanet:164736)
Fragile X syndrome (Orphanet:908)
Fragile X-associated tremor/ataxia syndrome (Orphanet:93256)
Gaucher disease (Orphanet:355)
Giant cell arteritis (Orphanet:397)
Glutaryl-CoA dehydrogenase deficiency (Orphanet:25)
Hartnup syndrome (Orphanet:2116)
Hereditary central diabetes insipidus (Orphanet:30925)
Holocarboxylase synthetase deficiency (Orphanet:79242)
Hurler syndrome (Orphanet:93473)
Hypernychthemeral syndrome (Orphanet:73267)
Hypoparathyroidism - deafness - renal disease (Orphanet:2237)
Indolent systemic mastocytosis (Orphanet:98848)
Kawasaki disease (Orphanet:2331)
Kleefstra syndrome (Orphanet:261494)
Kleefstra syndrome due to 9q34 microdeletion (Orphanet:96147)
Krabbe disease (Orphanet:487)
L1 syndrome (Orphanet:275543)
Marshall syndrome with periodic fever (Orphanet:42642)
Multiple endocrine neoplasia type 2 (Orphanet:653)
Nasu-Hakola disease (Orphanet:2770)
Non-polyposis Turcot syndrome (Orphanet:99817)
Norrie disease (Orphanet:649)
Oculocerebrorenal syndrome (Orphanet:534)
Pantothenate kinase-associated neurodegeneration (Orphanet:157850)
Perry syndrome (Orphanet:178509)
Posterior cortical atrophy (Orphanet:54247)
Progeria - short stature - pigmented nevi (Orphanet:2959)
Rabies (Orphanet:770)
Rett syndrome (Orphanet:778)
Rhabdoid tumor (Orphanet:69077)
Riboflavin transporter deficiency (Orphanet:97229)
Rubinstein-Taybi syndrome (Orphanet:783)
Schwartz-Jampel syndrome (Orphanet:800)
Smith-Magenis syndrome (Orphanet:819)
Symptomatic form of Coffin-Lowry syndrome in female carriers (Orphanet:276630)
Trisomy X (Orphanet:3375)
Usher syndrome (Orphanet:886)
Usher syndrome type 1 (Orphanet:231169)
Usher syndrome type 2 (Orphanet:231178)
Usher syndrome type 3 (Orphanet:231183)
Whipple disease (Orphanet:3452)
Williams syndrome (Orphanet:904)
Wolfram syndrome 2 (OMIM:604928)
X-linked creatine transporter deficiency (Orphanet:52503)