Abnormal emotion/affect behavior
Symptom Information:
Symptom ID: | HPO:0100851 | ||||||
Synonyms: |
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Cross references: |
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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) Behavioral abnormality(HPO:0000708) Abnormal emotion/affect behavior(HPO:0100851) MedDRA: |
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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) |