Constipation
Symptom Information:
Symptom ID: | HPO:0002019 | ||||||||||||||||||||||
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 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) |
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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) |