Hernia of the abdominal wall

Symptom Information:

Symptom ID: HPO:0004299
Abdominal wall hernia [Orphanet:17550]
Hernia of abdominal wall [HPO:0004299]
Hernia of abdominal cavity (disorder) [Orphanet:17550]
Hernia of anterior abdominal wall (disorder) [Orphanet:17550]
Hernia of abdominal wall (disorder) [Orphanet:17550]
Hernia of abdominal wall [Orphanet:17550]
Ventral Hernia [Orphanet:17550]
Hernia of abdominal cavity [Orphanet:17550]
Herniae [Orphanet:17550]
Hernia abdominal wall [Orphanet:17550]
Abdominal hernia [Orphanet:17550]
Ventral hernia [Orphanet:17550]
Abdominal hernia [MedDRA:10060954]
Abdominal hernia acquired [MedDRA:10060954]
Abdominal hernia NOS [MedDRA:10060954]
Abdominal hernia of specified site [MedDRA:10060954]
Abdominal herniation [MedDRA:10060954]
Epigastric hernia [MedDRA:10060954]
Hernia abdominal wall [MedDRA:10060954]
Other hernia of abdominal cavity without mention of obstruction or gangrene [MedDRA:10060954]
Other ventral hernia without mention of obstruction or gangrene [MedDRA:10060954]
Unspecified ventral hernia without mention of obstruction or gangrene [MedDRA:10060954]
Ventral hernia [MedDRA:10060954]
Ventral hernia without mention of obstruction or gangrene [MedDRA:10060954]
Rectus abdominis hernia [MedDRA:10060954]
Linea alba hernia [MedDRA:10060954]
Laparocele [MedDRA:10060954]
Abdominal wall hernia [OMIM:Abdominal wall hernia]
Hernia [MedDRA:10019909]
Cross references:
Orphanet:17550 "Herniae" [Orphanet:17550]
OMIM: "Abdominal wall hernia" [OMIM:Abdominal wall hernia]
UMLS:C1442978 "Hernia of abdominal wall" [Orphanet:17550]
UMLS:C0019326 "Ventral Hernia" [Orphanet:17550]
UMLS:C0178282 "Hernia of abdominal cavity" [Orphanet:17550]
Is a (Direct Parents):
Orphanet Abnormality of the abdominal wall
MedDRA Hernias NEC
HPO         Abdominal wall defect
HPO         Hernia
MedDRA Abdominal hernias, site unspecified
Is a (Whole tree): HPO:
    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)
       Abnormality of connective tissue(HPO:0003549)
             Hernia of the abdominal wall(HPO:0004299)
General disorders and administration site conditions(MedDRA:10018065)
    General system disorders NEC(MedDRA:10018073)
       Hernias NEC(MedDRA:10019910)
          Hernia of the abdominal wall(HPO:0004299)
Gastrointestinal disorders(MedDRA:10017947)
    Abdominal hernias and other abdominal wall conditions(MedDRA:10000073)
       Abdominal hernias, site unspecified(MedDRA:10000072)
          Hernia of the abdominal wall(HPO:0004299)
Database Frequency: 176 / 7739

All diseases associated with this symptom:

15q14 microdeletion syndrome (Orphanet:261190)
15q24 microdeletion syndrome (Orphanet:94065)
17p13.3 microduplication syndrome (Orphanet:217385)
1q21.1 microdeletion syndrome (Orphanet:250989)
2p15p16.1 microdeletion syndrome (Orphanet:261349)
2q31.1 microdeletion syndrome (Orphanet:251014)
3C syndrome (Orphanet:7)
48,XXXY syndrome (Orphanet:96263)
48,XXYY syndrome (Orphanet:10)
6p22 microdeletion syndrome (Orphanet:251046)
Aarskog-Scott syndrome (Orphanet:915)
Achondrogenesis (Orphanet:932)
Achondrogenesis type 1A (Orphanet:93299)
Achondrogenesis type 1B (Orphanet:93298)
Achondrogenesis type 2 (Orphanet:93296)
Acrocallosal syndrome (Orphanet:36)
Acrofacial dysostosis, Catania type (Orphanet:1786)
Acroosteolysis, dominant type (Orphanet:955)
Alpha-mannosidosis (Orphanet:61)
Androgen insensitivity syndrome (Orphanet:754)
Angelman syndrome (Orphanet:72)
Aniridia - absent patella (Orphanet:1069)
Anophthalmia - megalocornea - cardiopathy - skeletal anomalies (Orphanet:1101)
Arrhinia - choanal atresia - microphthalmia (Orphanet:1135)
Arterial tortuosity syndrome (Orphanet:3342)
Arthrogryposis with oculomotor limitation and electroretinal anomalies (Orphanet:1154)
Aspartylglucosaminuria (Orphanet:93)
Autosomal dominant Robinow syndrome (Orphanet:3107)
Autosomal dominant cutis laxa (Orphanet:90348)
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)
Beckwith-Wiedemann syndrome (Orphanet:116)
Bird headed-dwarfism, Montreal type (Orphanet:2617)
Bladder exstrophy (Orphanet:93930)
Blepharonasofacial malformation syndrome (Orphanet:1252)
Bohring-Opitz syndrome (Orphanet:97297)
Bone dysplasia, lethal Holmgren type (Orphanet:1842)
Brachydactyly - mesomelia - intellectual deficit - heart defects (Orphanet:1277)
Brachymorphism - onychodysplasia - dysphalangism (Orphanet:1292)
Brittle cornea syndrome (Orphanet:90354)
Cabezas syndrome (Orphanet:85293)
Cataract - aberrant oral frenula - growth delay (Orphanet:1373)
Cavernous hemangiomas of face - supraumbilical midline raphe (Orphanet:2124)
Cerebellar ataxia - ectodermal dysplasia (Orphanet:1174)
Cerebro-facio-thoracic dysplasia (Orphanet:1394)
Classical homocystinuria (Orphanet:394)
Coffin-Siris syndrome (Orphanet:1465)
Complete androgen insensitivity syndrome (Orphanet:99429)
Conductive deafness - malformed external ear (Orphanet:3216)
Craniofaciofrontodigital syndrome (Orphanet:363705)
Craniosynostosis - fibular aplasia (Orphanet:1533)
Cutis laxa (Orphanet:209)
De Barsy syndrome (Orphanet:2962)
Deafness - epiphyseal dysplasia - short stature (Orphanet:3218)
Dermato-cardio-skeletal syndrome, Borrone type (Orphanet:1266)
Dislocation of the hip - dysmorphism (Orphanet:2412)
Distal 22q11.2 microdeletion syndrome (Orphanet:261330)
Distal monosomy 3p (Orphanet:1620)
Distal monosomy 7q36 (Orphanet:1636)
Distal monosomy 9p (Orphanet:1642)
Distal trisomy 6p (Orphanet:1745)
Dyssegmental dysplasia, Silverman-Handmaker type (Orphanet:1865)
Ectodermal dysplasia - intellectual deficit - central nervous system malformation (Orphanet:1812)
Ehlers-Danlos syndrome type 1 (Orphanet:90309)
Ehlers-Danlos syndrome type 11 (Orphanet:2295)
Ehlers-Danlos syndrome type 2 (Orphanet:90318)
Ehlers-Danlos syndrome type 7B (Orphanet:99876)
Ehlers-Danlos syndrome with periventricular heterotopia (Orphanet:82004)
Ehlers-Danlos syndrome, arthrochalasic type (Orphanet:1899)
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 type (Orphanet:1900)
Ehlers-Danlos syndrome, vascular type (Orphanet:286)
Familial hypomagnesemia - hypercalciuria - nephrocalcinosis - severe ocular involvement (Orphanet:2196)
Femoral-facial syndrome (Orphanet:1988)
Fetal hydantoin syndrome (Orphanet:1912)
Flat face - microstomia - ear anomaly (Orphanet:1968)
Focal dermal hypoplasia (Orphanet:2092)
Freeman-Sheldon syndrome (Orphanet:2053)
GM1 gangliosidosis (Orphanet:354)
Geroderma osteodysplastica (Orphanet:2078)
Grix-Blankenship-Peterson syndrome (Orphanet:2099)
Hemihypertrophy (Orphanet:2128)
Hereditary hyperekplexia (Orphanet:3197)
Hirschsprung disease - nail hypoplasia - dysmorphism (Orphanet:2153)
Hurler syndrome (Orphanet:93473)
Hurler-Scheie syndrome (Orphanet:93476)
Hydrocephaly - low insertion umbilicus (Orphanet:2184)
Hyposmia - nasal and ocular hypoplasia - hypogonadotropic hypogonadism (Orphanet:2250)
Ichthyosis follicularis - alopecia - photophobia (Orphanet:2273)
Intellectual deficit - polydactyly - uncombable hair (Orphanet:3082)
Intellectual deficit - sparse hair - brachydactyly (Orphanet:3051)
Intellectual deficit, Wolff type (Orphanet:3080)
Intellectual deficit, X-linked - Dandy-Walker malformation - basal ganglia disease - Seizures (Orphanet:1568)
Intellectual deficit, X-linked - dysmorphism - cerebral atrophy (Orphanet:2958)
Intellectual deficit, X-linked - short stature - obesity (Orphanet:3055)
Intellectual deficit, X-linked, Armfield type (Orphanet:85276)
Intellectual deficit, X-linked, Pai type (Orphanet:85322)
Jacobsen syndrome (Orphanet:2308)
Joubert syndrome with hepatic defect (Orphanet:1454)
Joubert syndrome with orofaciodigital defect (Orphanet:2754)
Kleefstra syndrome (Orphanet:261494)
Kleefstra syndrome due to 9q34 microdeletion (Orphanet:96147)
Lambert syndrome (Orphanet:1296)
Lateral meningocele syndrome (Orphanet:2789)
Lenz-Majewski hyperostotic dwarfism (Orphanet:2658)
Lowry-MacLean syndrome (Orphanet:2409)
Malignant hyperthermia - arthrogryposis - torticollis (Orphanet:2215)
Marfan syndrome (Orphanet:558)
Menkes disease (Orphanet:565)
Micrencephaly - corpus callosum agenesis - abnormal genitalia (Orphanet:2508)
Mononen-Karnes-Senac syndrome (Orphanet:2565)
Monosomy 5p (Orphanet:281)
Monosomy 9p (Orphanet:261112)
Muckle-Wells syndrome (Orphanet:575)
Mucolipidosis type 2 (Orphanet:576)
Mucolipidosis type 3 (Orphanet:577)
Mucopolysaccharidosis type 1 (Orphanet:579)
Mucopolysaccharidosis type 2 (Orphanet:580)
Mucopolysaccharidosis type 3 (Orphanet:581)
Mucopolysaccharidosis type 4 (Orphanet:582)
Mucopolysaccharidosis type 6 (Orphanet:583)
Mucopolysaccharidosis type 7 (Orphanet:584)
Mullerian derivatives - lymphangiectasia - polydactyly (Orphanet:1655)
Multiple benign circumferential skin creases on limbs (Orphanet:2505)
Myhre syndrome (Orphanet:2588)
Neurogenic arthrogryposis multiplex congenita (Orphanet:1143)
Non-distal trisomy 13q (Orphanet:1702)
Occipital horn syndrome (Orphanet:198)
Oculocerebral hypopigmentation syndrome, Cross type (Orphanet:2719)
Oculocerebrorenal syndrome (Orphanet:534)
Osteogenesis imperfecta (Orphanet:666)
Osteoglophonic dwarfism (Orphanet:2645)
Perlman syndrome (Orphanet:2849)
Persistent Müllerian duct syndrome (Orphanet:2856)
Peters-plus syndrome (Orphanet:709)
Pfeiffer-Palm-Teller syndrome (Orphanet:2871)
Polydactyly-myopia syndrome (Orphanet:2917)
Pseudomyxoma peritonei (Orphanet:26790)
Ruvalcaba syndrome (Orphanet:3121)
SCARF syndrome (Orphanet:3134)
SHORT syndrome (Orphanet:3163)
Sakati-Nyhan syndrome (Orphanet:3128)
Schilbach-Rott syndrome (Orphanet:2353)
Schinzel-Giedion syndrome (Orphanet:798)
Schwartz-Jampel syndrome (Orphanet:800)
Short-limb skeletal dysplasia with severe combined immunodeficiency (Orphanet:935)
Shprintzen-Goldberg syndrome (Orphanet:2462)
Sialidosis type 1 (Orphanet:812)
Sialidosis type 2 (Orphanet:87876)
Simpson-Golabi-Behmel syndrome (Orphanet:373)
Splenogonadal fusion - limb defects - micrognathia (Orphanet:2063)
Steinert myotonic dystrophy (Orphanet:273)
Subaortic stenosis - short stature (Orphanet:3191)
Tel Hashomer camptodactyly syndrome (Orphanet:3292)
Telecanthus - hypertelorism - strabismus - pes cavus (Orphanet:3293)
Toriello-Carey syndrome (Orphanet:3338)
Trigonocephaly - short stature - developmental delay (Orphanet:3369)
Trisomy 13 (Orphanet:3378)
Trisomy 18 (Orphanet:3380)
Trisomy 20p (Orphanet:261318)
Trisomy Xq28 (Orphanet:1762)
Ulnar-mammary syndrome (Orphanet:3138)
VACTERL with hydrocephalus (Orphanet:3412)
WAGR syndrome (Orphanet:893)
Weaver syndrome (Orphanet:3447)
Williams syndrome (Orphanet:904)
Wolf-Hirschhorn syndrome (Orphanet:280)
Wrinkly skin syndrome (Orphanet:2834)
X-linked Ehlers-Danlos syndrome (Orphanet:75497)