Constipation

Symptom Information:

Symptom ID: HPO:0002019
Synonyms:
Costiveness [HPO:0002019]
Dyschezia [HPO:0002019]
Constipation (disorder) [Orphanet:27480]
Constipation [Orphanet:27480]
Constipation [OMIM:Constipation]
Constipation [MedDRA:10010774]
Constipation (excl faecal impaction) [MedDRA:10010774]
Iatrogenic constipation [MedDRA:10010774]
Obstipation [MedDRA:10010774]
Constipation aggravated [MedDRA:10010774]
Constipation (excl fecal impaction) [MedDRA:10010774]
Stools absent [MedDRA:10010774]
Constipation chronic [MedDRA:10010774]
Opioid induced constipation [MedDRA:10010774]
Slow transit constipation [MedDRA:10010774]
Chronic idiopathic constipation [MedDRA:10010774]
Constipation (64%) [OMIM:Constipation (64%)]
Constipation (in 1 of 3 patients) [OMIM:Constipation (in 1 of 3 patients)]
Constipation (in some patients) [OMIM:Constipation (in some patients)]
Constipation (reported in 1 family with a PDFGRA mutation) [OMIM:Constipation (reported in 1 family with a PDFGRA mutation)]
Constipation, chronic [OMIM:Constipation, chronic]
Dyschezia [MedDRA:10051244]
Quality:
Cross references:
Orphanet:27480 "Constipation" [Orphanet:27480]
OMIM: "Constipation" [OMIM:Constipation]
OMIM: "Constipation (64%)" [OMIM:Constipation (64%)]
OMIM: "Constipation (in 1 of 3 patients)" [OMIM:Constipation (in 1 of 3 patients)]
OMIM: "Constipation (in some patients)" [OMIM:Constipation (in some patients)]
OMIM: "Constipation (reported in 1 family with a PDFGRA mutation)" [OMIM:Constipation (reported in 1 family with a PDFGRA mutation)]
OMIM: "Constipation, chronic" [OMIM:Constipation, chronic]
UMLS:C0009806 "Constipation" [HPO:0002019]
UMLS:C0009806 "Constipation" [Orphanet:27480]
Is a (Direct Parents):
MedDRA Gastrointestinal atonic and hypomotility disorders NEC
MedDRA Gastrointestinal dyskinetic disorders
Orphanet Functional anomalies of the digestive system
HPO         Abdominal symptom
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the abdomen(HPO:0001438)
          Abdominal symptom(HPO:0011458)
             Constipation(HPO:0002019)
MedDRA:
Gastrointestinal disorders(MedDRA:10017947)
    Gastrointestinal motility and defaecation conditions(MedDRA:10017977)
       Gastrointestinal dyskinetic disorders(MedDRA:10017950)
          Constipation(HPO:0002019)
       Gastrointestinal atonic and hypomotility disorders NEC(MedDRA:10017933)
          Constipation(HPO:0002019)
Database Frequency: 194 / 7739
Resource:

All diseases associated with this symptom:

1p36 deletion syndrome (Orphanet:1606)
22q11.2 deletion syndrome (Orphanet:567)
2q23.1 microdeletion syndrome (Orphanet:228402)
48,XXXY syndrome (Orphanet:96263)
48,XXYY syndrome (Orphanet:10)
49,XXXXY syndrome (Orphanet:96264)
ANAL SPHINCTER MYOPATHY, INTERNAL (OMIM:105565)
ATTRV122I amyloidosis (Orphanet:85451)
Acute intermittent porphyria (Orphanet:79276)
Adiposis dolorosa (Orphanet:36397)
Adult-onset autosomal dominant leukodystrophy (Orphanet:99027)
Aicardi syndrome (Orphanet:50)
Alexander disease (Orphanet:58)
Alpha-N-acetylgalactosaminidase deficiency (Orphanet:3137)
Alpha-thalassemia - X-linked intellectual deficit syndrome (Orphanet:847)
Alström syndrome (Orphanet:64)
Angelman syndrome (Orphanet:72)
Aromatic L-amino acid decarboxylase deficiency (Orphanet:35708)
Athyreosis (Orphanet:95713)
Atypical Rett syndrome (Orphanet:3095)
Autosomal recessive spastic paraplegia type 44 (Orphanet:320401)
Autosomal recessive spastic paraplegia type 54 (Orphanet:320380)
Axial mesodermal dysplasia spectrum (Orphanet:1834)
BARTTER SYNDROME, ANTENATAL, TYPE 1 (OMIM:601678)
BARTTER SYNDROME, ANTENATAL, TYPE 2 (OMIM:241200)
Bartter syndrome (Orphanet:112)
Behr syndrome (Orphanet:1239)
Blepharophimosis-intellectual deficit syndrome due to UBE3B deficiency (Orphanet:329255)
Botulism (Orphanet:1267)
C syndrome (Orphanet:1308)
CARDIOFACIOCUTANEOUS SYNDROME 1 (OMIM:115150)
CHROMOSOME 4q32.1-q32.2 TRIPLICATION SYNDROME (OMIM:613603)
CYSTINOSIS, NEPHROPATHIC (OMIM:219800)
Cardiofaciocutaneous syndrome (Orphanet:1340)
Carpenter-Waziri syndrome (Orphanet:93973)
Central congenital hypothyroidism (Orphanet:226298)
Christianson syndrome (Orphanet:85278)
Chudley-Lowry-Hoar syndrome (Orphanet:93971)
Congenital hypothyroidism (Orphanet:442)
Congenital hypothyroidism due to developmental anomaly (Orphanet:95711)
Congenital hypothyroidism due to transplacental passage of maternal TSH-binding inhibitory antibodies (Orphanet:95715)
Cystinosis (Orphanet:213)
DDOST-CDG (Orphanet:300536)
DIABETES INSIPIDUS, NEPHROGENIC, AUTOSOMAL (OMIM:125800)
DIABETES INSIPIDUS, NEPHROGENIC, X-LINKED (OMIM:304800)
DIASTASIS RECTI AND WEAKNESS OF THE LINEA ALBA (OMIM:612198)
Desminopathy (Orphanet:98909)
Distomatosis (Orphanet:1685)
Dopa-responsive dystonia due to sepiapterin reductase deficiency (Orphanet:70594)
Dystrophic epidermolysis bullosa (Orphanet:303)
EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE 1 (OMIM:601776)
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2 (OMIM:300672)
Ehlers-Danlos syndrome, hypermobility type (Orphanet:285)
Ehlers-Danlos syndrome, musculocontractural type (Orphanet:2953)
Emanuel syndrome (Orphanet:96170)
Epidermolysis bullosa simplex, Dowling-Meara type (Orphanet:79396)
FG SYNDROME 2 (OMIM:300321)
Fabry disease (Orphanet:324)
Familial Mediterranean fever (Orphanet:342)
Familial advanced sleep-phase syndrome (Orphanet:164736)
Familial amyloid polyneuropathy (Orphanet:85447)
Familial caudal dysgenesis (Orphanet:1768)
Familial dysautonomia (Orphanet:1764)
Familial intestinal malrotation - facial anomalies (Orphanet:2454)
Familial thyroid dyshormonogenesis (Orphanet:95716)
Familial visceral myopathy (Orphanet:2604)
Fatal familial insomnia (Orphanet:466)
Floating-Harbor syndrome (Orphanet:2044)
Foodborne botulism (Orphanet:228371)
Gastrointestinal stromal tumor (Orphanet:44890)
Generalized congenital lipodystrophy with myopathy (Orphanet:228429)
HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 1 (OMIM:142623)
HOLOPROSENCEPHALY 2 (OMIM:157170)
HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 6 (OMIM:614450)
Haddad syndrome (Orphanet:99803)
Hereditary coproporphyria (Orphanet:79273)
Hereditary nonpolyposis colon cancer (Orphanet:144)
Hinman syndrome (Orphanet:84085)
Hirschsprung disease (Orphanet:388)
Holmes-Gang syndrome (Orphanet:93970)
Holoprosencephaly (Orphanet:2162)
Hurler syndrome (Orphanet:93473)
Hurler-Scheie syndrome (Orphanet:93476)
Hyperphosphatasia-intellectual deficiency syndrome (Orphanet:247262)
Hypothyroidism due to TSH receptor mutations (Orphanet:90673)
Hypothyroidism due to deficient transcription factors involved in pituitary development or function (Orphanet:226307)
Hypotonia-speech impairment-severe cognitive delay syndrome (Orphanet:371364)
Iatrogenic botulism (Orphanet:254509)
Idiopathic congenital hypothyroidism (Orphanet:95717)
Infant botulism (Orphanet:178478)
Infantile dystonia-parkinsonism (Orphanet:238455)
Infantile hypophosphatasia (Orphanet:247651)
Inhalational botulism (Orphanet:254504)
Isolated thyroid-stimulating hormone deficiency (Orphanet:90674)
Isolated thyrotropin-releasing hormone deficiency (Orphanet:238670)
Jacobsen syndrome (Orphanet:2308)
Juberg-Marsidi syndrome (Orphanet:93972)
Juvenile dermatomyositis (Orphanet:93672)
Kapur-Toriello syndrome (Orphanet:2328)
Kleefstra syndrome (Orphanet:261494)
LEIOMYOMATOSIS, DIFFUSE, WITH ALPORT SYNDROME (OMIM:308940)
LUBS X-LINKED MENTAL RETARDATION SYNDROME (OMIM:300260)
Leigh syndrome (Orphanet:506)
Liddle syndrome (Orphanet:526)
MELAS (Orphanet:550)
MITOCHONDRIAL DNA DEPLETION SYNDROME 1 (MNGIE TYPE) (OMIM:603041)
MITOCHONDRIAL DNA DEPLETION SYNDROME 4B (MNGIE TYPE) (OMIM:613662)
MYXEDEMA (OMIM:255900)
Malonic aciduria (Orphanet:943)
Maternally-inherited diabetes and deafness (Orphanet:225)
Mitochondrial neurogastrointestinal encephalomyopathy (Orphanet:298)
Mowat-Wilson syndrome (Orphanet:2152)
Mowat-Wilson syndrome due to a point mutation (Orphanet:261552)
Multiple endocrine neoplasia type 2 (Orphanet:653)
Multiple endocrine neoplasia type 2B (Orphanet:247709)
Muscular pseudohypertrophy - hypothyroidism (Orphanet:2349)
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VII (OMIM:615548)
Neonatal severe primary hyperparathyroidism (Orphanet:417)
Nephrogenic diabetes insipidus (Orphanet:223)
Neuroferritinopathy (Orphanet:157846)
Neurologic Waardenburg-Shah syndrome (Orphanet:163746)
Niemann-Pick disease type A (Orphanet:77292)
Non-polyposis Turcot syndrome (Orphanet:99817)
Noonan syndrome (Orphanet:648)
OPITZ-KAVEGGIA SYNDROME (OMIM:305450)
Ochoa syndrome (Orphanet:2704)
Oculocerebrofacial syndrome, Kaufman type (Orphanet:2707)
Oculocerebrorenal syndrome (Orphanet:534)
Ondine syndrome (Orphanet:661)
PARKINSON DISEASE, LATE-ONSET (OMIM:168600)
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL DOMINANT, 4 (OMIM:610131)
Pantothenate kinase-associated neurodegeneration (Orphanet:157850)
Paroxysmal extreme pain disorder (Orphanet:46348)
Perinatal lethal hypophosphatasia (Orphanet:247623)
Peripheral hypothyroidism (Orphanet:226310)
Peripheral resistance to thyroid hormones (Orphanet:97927)
Peritoneal cystic mesothelioma (Orphanet:168816)
Permanent congenital hypothyroidism (Orphanet:226292)
Pitt-Hopkins syndrome (Orphanet:2896)
Pitt-Hopkins-like syndrome 2 (OMIM:614325)
Polymyositis (Orphanet:732)
Porphyria (Orphanet:738)
Porphyria variegata (Orphanet:79473)
Primary congenital hypothyroidism without thyroid developmental anomaly (Orphanet:95714)
Primary erythermalgia (Orphanet:90026)
Primary peritoneal carcinoma (Orphanet:168829)
Propionic acidemia (Orphanet:35)
Proximal renal tubular acidosis (Orphanet:47159)
Proximal tubulopathy - diabetes mellitus - cerebellar ataxia (Orphanet:3390)
Prune belly syndrome (Orphanet:2970)
Pseudomyxoma peritonei (Orphanet:26790)
Qazi-Markouizos syndrome (Orphanet:3010)
RETT SYNDROME, CONGENITAL VARIANT (OMIM:613454)
Recessive dystrophic epidermolysis bullosa inversa (Orphanet:79409)
Recessive dystrophic epidermolysis bullosa-generalized other (Orphanet:89842)
Renier-Gabreels-Jasper syndrome (Orphanet:93975)
Resistance to thyrotropin-releasing hormone syndrome (Orphanet:99832)
Rett syndrome (Orphanet:778)
Rheumatic fever (Orphanet:3099)
Rubinstein-Taybi syndrome (Orphanet:783)
Rubinstein-Taybi syndrome due to CREBBP mutations (Orphanet:353277)
SCHAAF-YANG SYNDROME (OMIM:615547)
SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 1 (OMIM:604320)
STEVENSON-CAREY SYNDROME (OMIM:611961)
Scheie syndrome (Orphanet:93474)
Septo-optic dysplasia (Orphanet:3157)
Severe generalized recessive dystrophic epidermolysis bullosa (Orphanet:79408)
Smith-Fineman-Myers syndrome (Orphanet:93974)
Smith-Lemli-Opitz syndrome (Orphanet:818)
Smith-Magenis syndrome (Orphanet:819)
Sodium channelopathy-related small fiber neuropathy (Orphanet:306577)
Spinal muscular atrophy with respiratory distress (Orphanet:98920)
TETRAAMELIA WITH ECTODERMAL DYSPLASIA AND LACRIMAL DUCT ABNORMALITIES (OMIM:273390)
THYROID DYSHORMONOGENESIS 1 (OMIM:274400)
TMCO1 defect syndrome (Orphanet:228407)
TRAPS syndrome (Orphanet:32960)
Thyroid ectopia (Orphanet:95712)
Thyroid hemiagenesis (Orphanet:95719)
Thyroid hypoplasia (Orphanet:95720)
Timothy syndrome (Orphanet:65283)
Townes-Brocks syndrome (Orphanet:857)
Toxin-mediated infectious botulism (Orphanet:230800)
Transient congenital hypothyroidism (Orphanet:178045)
Typhoid (Orphanet:99745)
UROFACIAL SYNDROME 2 (OMIM:615112)
Visceral neuropathy - brain anomalies - facial dysmorphism - developmental delay (Orphanet:73246)
Waardenburg-Shah syndrome (Orphanet:897)
Wiedemann-Steiner syndrome (Orphanet:319182)
Williams syndrome (Orphanet:904)
Wolfram syndrome (Orphanet:3463)
Wolfram syndrome 1 (OMIM:222300)
Wound botulism (Orphanet:178475)
X-linked creatine transporter deficiency (Orphanet:52503)
X-linked intellectual deficit - hypotonic face (Orphanet:73220)