Irritability
Symptom Information:
| Symptom ID: | HPO:0000737 | ||||||||||||||||||
| Synonyms: |
|
||||||||||||||||||
| Quality: | |||||||||||||||||||
| Cross references: |
|
||||||||||||||||||
| 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) Irritability(HPO:0000737) MedDRA: General disorders and administration site conditions(MedDRA:10018065) General system disorders NEC(MedDRA:10018073) General signs and symptoms NEC(MedDRA:10018072) Irritability(HPO:0000737) |
||||||||||||||||||
| Database Frequency: | 93 / 7739 | ||||||||||||||||||
| Resource: |
All diseases associated with this symptom:
| 48,XXYY syndrome | (Orphanet:10) |
| 6-pyruvoyl-tetrahydropterin synthase deficiency | (Orphanet:13) |
| AICARDI-GOUTIERES SYNDROME 7 | (OMIM:615846) |
| Aceruloplasminemia | (Orphanet:48818) |
| Acrodermatitis enteropathica, zinc deficiency type | (Orphanet:37) |
| Adenylosuccinate lyase deficiency | (Orphanet:46) |
| Allan-Herndon-Dudley syndrome | (Orphanet:59) |
| Alström syndrome | (Orphanet:64) |
| Amish infantile epilepsy syndrome | (Orphanet:171714) |
| Amish lethal microcephaly | (Orphanet:99742) |
| Argininemia | (Orphanet:90) |
| Argininosuccinic aciduria | (Orphanet:23) |
| Aromatic L-amino acid decarboxylase deficiency | (Orphanet:35708) |
| Behçet disease | (Orphanet:117) |
| Blue diaper syndrome | (Orphanet:94086) |
| CADASIL | (Orphanet:136) |
| CK syndrome | (Orphanet:251383) |
| CLN1 disease | (Orphanet:228329) |
| COG4-CDG | (Orphanet:263501) |
| Carbamoylphosphate synthetase deficiency | (Orphanet:147) |
| Cardiofaciocutaneous syndrome | (Orphanet:1340) |
| Citrullinemia type I | (Orphanet:247525) |
| Citrullinemia type II | (Orphanet:247585) |
| Classical phenylketonuria | (Orphanet:79254) |
| Classical progressive supranuclear palsy | (Orphanet:240071) |
| Creutzfeldt-Jakob disease | (Orphanet:204) |
| Cushing disease | (Orphanet:96253) |
| Cushing syndrome | (Orphanet:553) |
| D,L-2-hydroxyglutaric aciduria | (Orphanet:356978) |
| DIABETES INSIPIDUS, NEPHROGENIC, AUTOSOMAL | (OMIM:125800) |
| DIABETES INSIPIDUS, NEPHROGENIC, X-LINKED | (OMIM:304800) |
| Dihydropteridine reductase deficiency | (Orphanet:226) |
| Dopa-responsive dystonia due to sepiapterin reductase deficiency | (Orphanet:70594) |
| Dyschromatosis symmetrica hereditaria | (Orphanet:41) |
| EDEMA, FAMILIAL IDIOPATHIC, PREPUBERTAL | (OMIM:129840) |
| EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 15 | (OMIM:615006) |
| FRONTOTEMPORAL DEMENTIA | (OMIM:600274) |
| Familial hemophagocytic lymphohistiocytosis | (Orphanet:540) |
| Familial isolated dilated cardiomyopathy | (Orphanet:154) |
| Farber lipogranulomatosis | (Orphanet:333) |
| Frontotemporal dementia | (Orphanet:282) |
| Fructose-1,6-bisphosphatase deficiency | (Orphanet:348) |
| GRAVES DISEASE, SUSCEPTIBILITY TO, 1 | (OMIM:275000) |
| GTP cyclohydrolase I deficiency | (Orphanet:2102) |
| Gaucher disease type 2 | (Orphanet:77260) |
| Glycine encephalopathy | (Orphanet:407) |
| HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 1 | (OMIM:267700) |
| HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 2 | (OMIM:603553) |
| HYPERPHOSPHATEMIA, POLYURIA, AND SEIZURES | (OMIM:239350) |
| HYPOGLYCEMIA, LEUCINE-INDUCED | (OMIM:240800) |
| Hereditary folate malabsorption | (Orphanet:90045) |
| Holocarboxylase synthetase deficiency | (Orphanet:79242) |
| Huntington disease | (Orphanet:399) |
| Huntington disease-like 2 | (Orphanet:98934) |
| Hyperammonemia due to N-acetylglutamate synthetase deficiency | (Orphanet:927) |
| Hypermethioninemia encephalopathy due to adenosine kinase deficiency | (Orphanet:289290) |
| Hypocalcemic vitamin D-dependent rickets | (Orphanet:289157) |
| Hypocalcemic vitamin D-resistant rickets | (Orphanet:93160) |
| Infantile hypophosphatasia | (Orphanet:247651) |
| Inherited Creutzfeldt-Jakob disease | (Orphanet:282166) |
| Joubert syndrome 14 | (OMIM:614424) |
| Letterer-Siwe disease | (Orphanet:99870) |
| MELAS | (Orphanet:550) |
| MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 4 | (OMIM:615228) |
| Maternal hyperphenylalaninemia | (Orphanet:2209) |
| Mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria | (Orphanet:1933) |
| Mitochondrial DNA depletion syndrome, myopathic form | (Orphanet:254875) |
| Mohr-Tranebjaerg syndrome | (Orphanet:52368) |
| NEUROPATHY, HEREDITARY SENSORY, TYPE IE | (OMIM:614116) |
| Nasu-Hakola disease | (Orphanet:2770) |
| Neonatal hemochromatosis | (Orphanet:446) |
| Nephrogenic diabetes insipidus | (Orphanet:223) |
| Nephrogenic syndrome of inappropriate antidiuresis | (Orphanet:93606) |
| Nephronophthisis 1 | (OMIM:256100) |
| Ornithine transcarbamylase deficiency | (Orphanet:664) |
| PICK DISEASE OF BRAIN | (OMIM:172700) |
| POLYMYOCLONUS, INFANTILE | (OMIM:263550) |
| PONTOCEREBELLAR HYPOPLASIA, TYPE 2D | (OMIM:613811) |
| PONTOCEREBELLAR HYPOPLASIA, TYPE 2E | (OMIM:615851) |
| Paroxysmal exertion-induced dyskinesia | (Orphanet:98811) |
| Perinatal lethal hypophosphatasia | (Orphanet:247623) |
| Peroxisomal acyl-CoA oxidase deficiency | (Orphanet:2971) |
| Pontocerebellar hypoplasia, type 9 | (OMIM:615809) |
| Progressive epilepsy-intellectual deficit, Finnish type | (Orphanet:1947) |
| Pyruvate dehydrogenase E3-binding protein deficiency | (Orphanet:255182) |
| Pyruvate dehydrogenase phosphatase deficiency | (Orphanet:79246) |
| SUPRANUCLEAR PALSY, PROGRESSIVE, 1 | (OMIM:601104) |
| SUPRANUCLEAR PALSY, PROGRESSIVE, 2 | (OMIM:609454) |
| Thiamine-responsive encephalopathy | (Orphanet:199348) |
| Transcobalamin deficiency | (Orphanet:859) |
| VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1A | (OMIM:264700) |
| VITAMIN D-DEPENDENT RICKETS, TYPE 2A | (OMIM:277440) |
| Very long chain acyl-CoA dehydrogenase deficiency | (Orphanet:26793) |