Umbilical hernia

Symptom Information:

Symptom ID: HPO:0001537
Synonyms:
Umbilical hernias [HPO:0001537]
Umbilical hernia (disorder) [Orphanet:17770]
Umbilical hernia without mention of obstruction or gangrene [Orphanet:17770]
Umbilical hernia [Orphanet:17770]
Umbilical hernia [OMIM:Umbilical hernia]
Umbilical hernias [OMIM:Umbilical hernias]
Exomphalos [Orphanet:17770]
Umbilical hernia [MedDRA:10045458]
Para-umbilical hernia [MedDRA:10045458]
Umbilical hernia NOS [MedDRA:10045458]
Umbilical hernia without mention of obstruction or gangrene [MedDRA:10045458]
Exomphalos [MedDRA:10015677]
Omphalocele [MedDRA:10015677]
Omphalocoele [MedDRA:10015677]
Omphalocele (exomphalos) [OMIM:Omphalocele (exomphalos)]
Omphalocele (in some patients) [OMIM:Omphalocele (in some patients)]
Omphalocele (males) [OMIM:Omphalocele (males)]
Omphalocele (rare) [OMIM:Omphalocele (rare)]
Omphalocele (rare, in males) [OMIM:Omphalocele (rare, in males)]
Omphalocele. [OMIM:Omphalocele.]
Umbilical hernia (32%) [OMIM:Umbilical hernia (32%)]
Umbilical hernia (in some patients) [OMIM:Umbilical hernia (in some patients)]
Umbilical hernia (rare) [OMIM:Umbilical hernia (rare)]
Umbilical hernias [MedDRA:10045459]
Quality:
Cross references:
Orphanet:17770 "Umbilical hernia" [Orphanet:17770]
OMIM: "Umbilical hernia" [OMIM:Umbilical hernia]
OMIM: "Umbilical hernias" [OMIM:Umbilical hernias]
OMIM: "Omphalocele (exomphalos)" [OMIM:Omphalocele (exomphalos)]
OMIM: "Omphalocele (in some patients)" [OMIM:Omphalocele (in some patients)]
OMIM: "Omphalocele (males)" [OMIM:Omphalocele (males)]
OMIM: "Omphalocele (rare)" [OMIM:Omphalocele (rare)]
OMIM: "Omphalocele (rare, in males)" [OMIM:Omphalocele (rare, in males)]
OMIM: "Omphalocele." [OMIM:Omphalocele.]
OMIM: "Umbilical hernia (32%)" [OMIM:Umbilical hernia (32%)]
OMIM: "Umbilical hernia (in some patients)" [OMIM:Umbilical hernia (in some patients)]
OMIM: "Umbilical hernia (rare)" [OMIM:Umbilical hernia (rare)]
UMLS:C0041636 "Umbilical hernia without mention of obstruction or gangrene" [Orphanet:17770]
UMLS:C0019322 "Umbilical hernia" [Orphanet:17770]
Is a (Direct Parents):
HPO         Abnormality of the umbilicus
Orphanet Hernia of the abdominal wall
MedDRA Abdominal hernias and other abdominal wall conditions
HPO         Hernia of the abdominal wall
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the abdomen(HPO:0001438)
          Abnormality of the abdominal wall(HPO:0004298)
             Abdominal wall defect(HPO:0010866)
                Hernia of the abdominal wall(HPO:0004299)
                   Umbilical hernia(HPO:0001537)
             Abnormality of the umbilicus(HPO:0001551)
                Umbilical hernia(HPO:0001537)
       Abnormality of connective tissue(HPO:0003549)
          Hernia(HPO:0100790)
             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)
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)