Umbilical hernia
Symptom Information:
Symptom ID: | HPO:0001537 | ||||||||||||||||||||||||
Synonyms: |
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Quality: | |||||||||||||||||||||||||
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 connective tissue(HPO:0003549) Hernia(HPO:0100790) Hernia of the abdominal wall(HPO:0004299) Umbilical hernia(HPO:0001537) Abnormality of the abdomen(HPO:0001438) Abnormality of the abdominal wall(HPO:0004298) Abnormality of the umbilicus(HPO:0001551) Umbilical hernia(HPO:0001537) Abdominal wall defect(HPO:0010866) Hernia of the abdominal wall(HPO:0004299) Umbilical hernia(HPO:0001537) MedDRA: Gastrointestinal disorders(MedDRA:10017947) Abdominal hernias and other abdominal wall conditions(MedDRA:10000073) Umbilical hernia(HPO:0001537) |
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Database Frequency: | 206 / 7739 | ||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
22q11.2 deletion syndrome | (Orphanet:567) |
2q37 microdeletion syndrome | (Orphanet:1001) |
3C syndrome | (Orphanet:7) |
ADAMS-OLIVER SYNDROME 4 | (OMIM:615297) |
ADAMS-OLIVER SYNDROME 5 | (OMIM:616028) |
AGONADISM, 46,XY, WITH MENTAL RETARDATION, SHORT STATURE, RETARDEDBONE AGE, AND MULTIPLE EXTRAGENITAL MALFORMATIONS | (OMIM:600908) |
ALDH18A1-related De Barsy syndrome | (Orphanet:35664) |
AMASTIA, BILATERAL, WITH URETERAL TRIPLICATION AND DYSMORPHISM | (OMIM:104350) |
AXENFELD-RIEGER SYNDROME, TYPE 2 | (OMIM:601499) |
Aarskog-Scott syndrome | (Orphanet:915) |
Ablepharon macrostomia syndrome | (Orphanet:920) |
Achondrogenesis | (Orphanet:932) |
Achondrogenesis type 1A | (Orphanet:93299) |
Achondrogenesis type 1B | (Orphanet:93298) |
Achondrogenesis type 2 | (Orphanet:93296) |
Acrocallosal syndrome | (Orphanet:36) |
Acrocephalopolydactyly | (Orphanet:221054) |
Acroosteolysis, dominant type | (Orphanet:955) |
Alpha-mannosidosis | (Orphanet:61) |
Alpha-thalassemia - X-linked intellectual deficit syndrome | (Orphanet:847) |
Aneurysm - osteoarthritis syndrome | (Orphanet:284984) |
Aniridia | (Orphanet:77) |
Anophthalmia - megalocornea - cardiopathy - skeletal anomalies | (Orphanet:1101) |
Arachnodactyly - abnormal ossification - intellectual deficit | (Orphanet:1129) |
Arterial tortuosity syndrome | (Orphanet:3342) |
Aspartylglucosaminuria | (Orphanet:93) |
Autosomal dominant Opitz G/BBB syndrome | (Orphanet:306588) |
Autosomal dominant Robinow syndrome | (Orphanet:3107) |
Autosomal recessive Robinow syndrome | (Orphanet:1507) |
Autosomal recessive cutis laxa type 1 | (Orphanet:90349) |
Autosomal recessive cutis laxa type 2 | (Orphanet:90350) |
Autosomal recessive multiple pterygium syndrome | (Orphanet:2990) |
Autosomal recessive omodysplasia | (Orphanet:93329) |
Autosomal recessive spondylocostal dysostosis | (Orphanet:2311) |
BRESEK syndrome | (Orphanet:85284) |
BRITTLE CORNEA SYNDROME 2 | (OMIM:614170) |
Beckwith-Wiedemann syndrome | (Orphanet:116) |
Beckwith-Wiedemann syndrome due to 11p15 microdeletion | (Orphanet:231127) |
Beckwith-Wiedemann syndrome due to 11p15 microduplication | (Orphanet:96076) |
Beckwith-Wiedemann syndrome due to 11p15 translocation/inversion | (Orphanet:231130) |
Beckwith-Wiedemann syndrome due to CDKN1C mutation | (Orphanet:231120) |
Beckwith-Wiedemann syndrome due to NSD1 mutation | (Orphanet:238613) |
Beckwith-Wiedemann syndrome due to imprinting defect of 11p15 | (Orphanet:231117) |
Beckwith-Wiedemann syndrome due to paternal uniparental disomy of chromosome 11 | (Orphanet:96193) |
Bladder exstrophy | (Orphanet:93930) |
Brachymorphism - onychodysplasia - dysphalangism | (Orphanet:1292) |
CARPENTER SYNDROME 1 | (OMIM:201000) |
CARPENTER SYNDROME 2 | (OMIM:614976) |
CATEL-MANZKE SYNDROME | (OMIM:616145) |
CHARGE syndrome | (Orphanet:138) |
CHILD syndrome | (Orphanet:139) |
CHROMOSOME 6q11-q14 DELETION SYNDROMECHROMOSOME 6q13-q14 DELETION SYNDROME, INCLUDED | (OMIM:613544) |
COFFIN-SIRIS SYNDROME | (OMIM:135900) |
CONGENITAL CONTRACTURES OF THE LIMBS AND FACE, HYPOTONIA, AND DEVELOPMENTALDELAY | (OMIM:616266) |
CRANIOSYNOSTOSIS-MENTAL RETARDATION SYNDROME OF LIN AND GETTIG | (OMIM:218649) |
CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IA | (OMIM:219100) |
Cardiofaciocutaneous syndrome | (Orphanet:1340) |
Carpenter syndrome | (Orphanet:65759) |
Cataract - aberrant oral frenula - growth delay | (Orphanet:1373) |
Catel-Manzke syndrome | (Orphanet:1388) |
Central congenital hypothyroidism | (Orphanet:226298) |
Coffin-Siris syndrome | (Orphanet:1465) |
Combined immunodeficiency with facio-oculo-skeletal anomalies | (Orphanet:221139) |
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) |
Cooper-Jabs syndrome | (Orphanet:1488) |
Craniofacial dyssynostosis | (Orphanet:1516) |
Craniofaciofrontodigital syndrome | (Orphanet:363705) |
Craniofrontonasal dysplasia | (Orphanet:1520) |
Craniosynostosis - hydrocephalus - Chiari I malformation - radioulnar synostosis | (Orphanet:171839) |
Cutis gyrata - acanthosis nigricans - craniosynostosis | (Orphanet:1555) |
Cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies | (Orphanet:221145) |
DIGEORGE SYNDROME | (OMIM:188400) |
De Barsy syndrome | (Orphanet:2962) |
Deafness - epiphyseal dysplasia - short stature | (Orphanet:3218) |
Deafness - intellectual deficit, Martin-Probst type | (Orphanet:85321) |
Dent disease type 2 | (Orphanet:93623) |
Dermato-cardio-skeletal syndrome, Borrone type | (Orphanet:1266) |
Distal monosomy 19p13.3 | (Orphanet:96129) |
Distal monosomy 3p | (Orphanet:1620) |
Donnai-Barrow syndrome | (Orphanet:2143) |
Down syndrome | (Orphanet:870) |
Dyssegmental dysplasia, Silverman-Handmaker type | (Orphanet:1865) |
EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE 1 | (OMIM:601776) |
ENCEPHALOMYOPATHY, MITOCHONDRIAL, DUE TO VOLTAGE-DEPENDENT ANION CHANNELDEFICIENCY | (OMIM:614520) |
Ehlers-Danlos syndrome type 1 | (Orphanet:90309) |
Ehlers-Danlos syndrome type 2 | (Orphanet:90318) |
Ehlers-Danlos syndrome, classic type | (Orphanet:287) |
Ehlers-Danlos syndrome, dermatosparaxis type | (Orphanet:1901) |
Ehlers-Danlos syndrome, hypermobility type | (Orphanet:285) |
Ehlers-Danlos syndrome, kyphoscoliotic and deafness type | (Orphanet:300179) |
Ehlers-Danlos syndrome, musculocontractural type | (Orphanet:2953) |
Ehlers-Danlos syndrome, vascular type | (Orphanet:286) |
Encephalopathy due to beta-mercaptolactate-cysteine disulfiduria | (Orphanet:1035) |
Facial dysmorphism - shawl scrotum - joint laxity | (Orphanet:1778) |
Familial hypomagnesemia - hypercalciuria - nephrocalcinosis - severe ocular involvement | (Orphanet:2196) |
Familial thyroid dyshormonogenesis | (Orphanet:95716) |
Familial visceral myopathy | (Orphanet:2604) |
Fanconi anemia | (Orphanet:84) |
Fetal minoxidil syndrome | (Orphanet:1918) |
Floating-Harbor syndrome | (Orphanet:2044) |
Focal dermal hypoplasia | (Orphanet:2092) |
Fraser syndrome | (Orphanet:2052) |
GAPO syndrome | (Orphanet:2067) |
Gaucher disease type 2 | (Orphanet:77260) |
Gonadal dysgenesis, XY type - associated anomalies | (Orphanet:1770) |
Gorlin-Chaudhry-Moss syndrome | (Orphanet:2095) |
Greig cephalopolysyndactyly syndrome | (Orphanet:380) |
HAJDU-CHENEY SYNDROME | (OMIM:102500) |
HUNTER-MACDONALD SYNDROME | (OMIM:611962) |
HYPEREKPLEXIA, HEREDITARY 1 | (OMIM:149400) |
Hennekam syndrome | (Orphanet:2136) |
Hereditary hyperekplexia | (Orphanet:3197) |
Holoprosencephaly - postaxial polydactyly | (Orphanet:2166) |
Hurler syndrome | (Orphanet:93473) |
Hurler-Scheie syndrome | (Orphanet:93476) |
Hydrocephaly - tall stature - joint laxity | (Orphanet:2181) |
Hypertelorism, Teebi type | (Orphanet:1519) |
Hypertrichotic osteochondrodysplasia, Cantu type | (Orphanet:1517) |
Hypothyroidism due to TSH receptor mutations | (Orphanet:90673) |
Hypothyroidism due to deficient transcription factors involved in pituitary development or function | (Orphanet:226307) |
ICF syndrome | (Orphanet:2268) |
Ichthyosis follicularis - alopecia - photophobia | (Orphanet:2273) |
Incontinentia pigmenti | (Orphanet:464) |
Insulin-resistance syndrome type A | (Orphanet:2297) |
Intellectual deficit - hypotonia - skin hyperpigmentation | (Orphanet:3050) |
Intellectual deficit, Buenos-Aires type | (Orphanet:3079) |
Isolated thyroid-stimulating hormone deficiency | (Orphanet:90674) |
Kleefstra syndrome due to 9q34 microdeletion | (Orphanet:96147) |
Kniest dysplasia | (Orphanet:485) |
LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 1 | (OMIM:608594) |
LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 2 | (OMIM:269700) |
LOEYS-DIETZ SYNDROME 2 | (OMIM:610168) |
Lateral meningocele syndrome | (Orphanet:2789) |
Leprechaunism | (Orphanet:508) |
Lethal polymalformative syndrome, Boissel type | (Orphanet:210144) |
Leukocyte adhesion deficiency | (Orphanet:2968) |
MACS syndrome | (Orphanet:217335) |
MUSCULAR HYPERTONIA, LETHAL | (OMIM:254120) |
Marshall-Smith syndrome | (Orphanet:561) |
Megacystis-microcolon-intestinal hypoperistalsis syndrome | (Orphanet:2241) |
Menkes disease | (Orphanet:565) |
Mesomelia-synostoses syndrome | (Orphanet:2496) |
Mitochondrial encephalo-cardio-myopathy due to TMEM70 deficiency | (Orphanet:1194) |
Monosomy 18q | (Orphanet:1600) |
Monosomy 22q13 | (Orphanet:48652) |
Monosomy 9q22.3 | (Orphanet:77301) |
Mucolipidosis type 2 | (Orphanet:576) |
Mucopolysaccharidosis type 1 | (Orphanet:579) |
Mucopolysaccharidosis type 2 | (Orphanet:580) |
Mucopolysaccharidosis type 2, attenuated form | (Orphanet:217093) |
Mucopolysaccharidosis type 2, severe form | (Orphanet:217085) |
Mucopolysaccharidosis type 3 | (Orphanet:581) |
Mucopolysaccharidosis type 6 | (Orphanet:583) |
Mucopolysaccharidosis type 7 | (Orphanet:584) |
Multiple benign circumferential skin creases on limbs | (Orphanet:2505) |
Multiple intestinal atresia | (Orphanet:2300) |
Muscular pseudohypertrophy - hypothyroidism | (Orphanet:2349) |
Noonan syndrome-like disorder with loose anagen hair | (Orphanet:2701) |
OPITZ-KAVEGGIA SYNDROME | (OMIM:305450) |
OSTEOGENESIS IMPERFECTA, TYPE XIII | (OMIM:614856) |
Oculocerebrorenal syndrome | (Orphanet:534) |
Oculodentodigital dysplasia | (Orphanet:2710) |
Oculofaciocardiodental syndrome | (Orphanet:2712) |
Opitz G/BBB syndrome | (Orphanet:2745) |
Osteodysplasty, Melnick-Needles type | (Orphanet:2484) |
Osteogenesis imperfecta | (Orphanet:666) |
Osteopathia striata - cranial sclerosis | (Orphanet:2780) |
PELGER-HUET ANOMALY | (OMIM:169400) |
PSYCHOMOTOR RETARDATION, EPILEPSY, AND CRANIOFACIAL DYSMORPHISM | (OMIM:614501) |
Pancreatic hypoplasia - diabetes - congenital heart disease | (Orphanet:2255) |
Peripheral hypothyroidism | (Orphanet:226310) |
Peripheral resistance to thyroid hormones | (Orphanet:97927) |
Permanent congenital hypothyroidism | (Orphanet:226292) |
Peters-plus syndrome | (Orphanet:709) |
Primary congenital hypothyroidism | (Orphanet:226295) |
Primary congenital hypothyroidism without thyroid developmental anomaly | (Orphanet:95714) |
Progeroid syndrome, Petty type | (Orphanet:2963) |
Pseudoaminopterin syndrome | (Orphanet:221120) |
Pyruvate dehydrogenase E1-alpha deficiency | (Orphanet:79243) |
ROBINOW SYNDROME, AUTOSOMAL DOMINANT 2 | (OMIM:616331) |
Renal-genital-middle ear anomalies | (Orphanet:1092) |
Resistance to thyrotropin-releasing hormone syndrome | (Orphanet:99832) |
SCARF syndrome | (Orphanet:3134) |
SENER SYNDROME | (OMIM:606156) |
Scheie syndrome | (Orphanet:93474) |
Schwartz-Jampel syndrome | (Orphanet:800) |
Shprintzen-Goldberg syndrome | (Orphanet:2462) |
Simpson-Golabi-Behmel syndrome | (Orphanet:373) |
TATTON-BROWN-RAHMAN SYNDROME | (OMIM:615879) |
TETRAAMELIA WITH ECTODERMAL DYSPLASIA AND LACRIMAL DUCT ABNORMALITIES | (OMIM:273390) |
THYROID DYSHORMONOGENESIS 1 | (OMIM:274400) |
Tetrasomy 12p | (Orphanet:884) |
Thyroid ectopia | (Orphanet:95712) |
Thyroid hemiagenesis | (Orphanet:95719) |
Toriello-Carey syndrome | (Orphanet:3338) |
Townes-Brocks syndrome | (Orphanet:857) |
Trisomy 20p | (Orphanet:261318) |
VELOCARDIOFACIAL SYNDROME | (OMIM:192430) |
Weaver syndrome | (Orphanet:3447) |
Williams syndrome | (Orphanet:904) |
Wilson-Turner syndrome | (Orphanet:3459) |
Wrinkly skin syndrome | (Orphanet:2834) |
X-linked Ehlers-Danlos syndrome | (Orphanet:75497) |
Zimmermann-Laband syndrome | (Orphanet:3473) |