Inguinal hernia

Symptom Information:

Symptom ID: HPO:0000023
Synonyms:
Inguinoscrotal hernia [Orphanet:17660]
Inguinal hernia (disorder) [Orphanet:17660]
Hernia, Inguinal [Orphanet:17660]
Inguinal hernia [OMIM:Inguinal hernia]
Inguinal/inguinoscrotal/crural hernia [Orphanet:17660]
Inguinal hernia [Orphanet:17660]
Inguinal hernia [MedDRA:10022016]
Bilateral inguinal hernia, without mention of obstruction or gangrene [MedDRA:10022016]
Direct inguinal hernia [MedDRA:10022016]
Double inguinal hernia [MedDRA:10022016]
Hernia inguinal [MedDRA:10022016]
Indirect inguinal hernia [MedDRA:10022016]
Inguinal hernia NOS [MedDRA:10022016]
Inguinal hernia, without mention of obstruction or gangrene [MedDRA:10022016]
Left inguinal hernia [MedDRA:10022016]
Oblique inguinal hernia [MedDRA:10022016]
Recurrent bilateral inguinal hernia, without mention of obstruction or gangrene [MedDRA:10022016]
Recurrent unilateral or unspecified inguinal hernia, without mention of obstruction or gangrene [MedDRA:10022016]
Right inguinal hernia [MedDRA:10022016]
Scrotal hernia [MedDRA:10022016]
Sliding inguinal hernia [MedDRA:10022016]
Unilateral or unspecified inguinal hernia, without mention of obstruction or gangrene [MedDRA:10022016]
Bubonocele [MedDRA:10022016]
Bilateral inguinal hernia [MedDRA:10022016]
Bilateral inguinal hernia [OMIM:Bilateral inguinal hernia]
Inguinal hernia (17%) [OMIM:Inguinal hernia (17%)]
Inguinal hernia (21%) [OMIM:Inguinal hernia (21%)]
Inguinal hernia (in some patients) [OMIM:Inguinal hernia (in some patients)]
Inguinal hernia (rare) [OMIM:Inguinal hernia (rare)]
Inguinal hernia (some) [OMIM:Inguinal hernia (some)]
Inguinal hernia (type II, congenital) [OMIM:Inguinal hernia (type II, congenital)]
Inguinal hernia, bilateral [OMIM:Inguinal hernia, bilateral]
Inguinal herniae [OMIM:Inguinal herniae]
Inguinal hernias [OMIM:Inguinal hernias]
Inguinal hernias [MedDRA:10022017]
Quality:
Cross references:
Orphanet:17660 "Inguinal/inguinoscrotal/crural hernia" [Orphanet:17660]
OMIM: "Inguinal hernia" [OMIM:Inguinal hernia]
OMIM: "Bilateral inguinal hernia" [OMIM:Bilateral inguinal hernia]
OMIM: "Inguinal hernia (17%)" [OMIM:Inguinal hernia (17%)]
OMIM: "Inguinal hernia (21%)" [OMIM:Inguinal hernia (21%)]
OMIM: "Inguinal hernia (in some patients)" [OMIM:Inguinal hernia (in some patients)]
OMIM: "Inguinal hernia (rare)" [OMIM:Inguinal hernia (rare)]
OMIM: "Inguinal hernia (some)" [OMIM:Inguinal hernia (some)]
OMIM: "Inguinal hernia (type II, congenital)" [OMIM:Inguinal hernia (type II, congenital)]
OMIM: "Inguinal hernia, bilateral" [OMIM:Inguinal hernia, bilateral]
OMIM: "Inguinal herniae" [OMIM:Inguinal herniae]
OMIM: "Inguinal hernias" [OMIM:Inguinal hernias]
UMLS:C0019294 "Hernia, Inguinal" [Orphanet:17660]
Is a (Direct Parents):
MedDRA Abdominal hernias and other abdominal wall conditions
HPO         Hernia of the abdominal wall
Orphanet 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)
                   Inguinal hernia(HPO:0000023)
       Abnormality of connective tissue(HPO:0003549)
          Hernia(HPO:0100790)
             Hernia of the abdominal wall(HPO:0004299)
                Inguinal hernia(HPO:0000023)
MedDRA:
Gastrointestinal disorders(MedDRA:10017947)
    Abdominal hernias and other abdominal wall conditions(MedDRA:10000073)
       Inguinal hernia(HPO:0000023)
Database Frequency: 181 / 7739
Resource:

All diseases associated with this symptom:

15q24 microdeletion syndrome (Orphanet:94065)
22q11.2 deletion syndrome (Orphanet:567)
2q32q33 microdeletion syndrome (Orphanet:251019)
3-methylglutaconic aciduria type 4 (Orphanet:67048)
3C syndrome (Orphanet:7)
48,XXYY syndrome (Orphanet:10)
AARSKOG-SCOTT SYNDROME (OMIM:305400)
ADAMS-OLIVER SYNDROME 5 (OMIM:616028)
ALDH18A1-related De Barsy syndrome (Orphanet:35664)
ANDROGEN INSENSITIVITY SYNDROME (OMIM:300068)
ARTHROGRYPOSIS, DISTAL, TYPE 2A (OMIM:193700)
AXENFELD-RIEGER SYNDROME, TYPE 2 (OMIM:601499)
Achondrogenesis type 1B (Orphanet:93298)
Acrocallosal syndrome (Orphanet:36)
Alpha-mannosidosis (Orphanet:61)
Aneurysm - osteoarthritis syndrome (Orphanet:284984)
Arterial tortuosity syndrome (Orphanet:3342)
Autosomal dominant Opitz G/BBB syndrome (Orphanet:306588)
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 2A (Orphanet:357058)
Autosomal recessive facio-digito-genital syndrome (Orphanet:1974)
Autosomal recessive multiple pterygium syndrome (Orphanet:2990)
Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency (Orphanet:331176)
BARATELA-SCOTT SYNDROME (OMIM:300881)
BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA (OMIM:609945)
BRESEK syndrome (Orphanet:85284)
BRITTLE CORNEA SYNDROME 2 (OMIM:614170)
BRUCK SYNDROME 2 (OMIM:609220)
Beckwith-Wiedemann syndrome due to CDKN1C mutation (Orphanet:231120)
Beckwith-Wiedemann syndrome due to imprinting defect of 11p15 (Orphanet:231117)
Bladder exstrophy (Orphanet:93930)
CARDIAC VALVULAR DEFECT, DEVELOPMENTAL (OMIM:212093)
CATEL-MANZKE SYNDROME (OMIM:616145)
CHROMOSOME 15q25 DELETION SYNDROME (OMIM:614294)
CHROMOSOME 1p32-p31 DELETION SYNDROME (OMIM:613735)
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)
CORNEAL DYSTROPHY, POSTERIOR POLYMORPHOUS, 3 (OMIM:609141)
CRANIOSYNOSTOSIS-MENTAL RETARDATION SYNDROME OF LIN AND GETTIG (OMIM:218649)
CUTIS LAXA, AUTOSOMAL DOMINANT 1 (OMIM:123700)
CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IA (OMIM:219100)
CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IB (OMIM:614437)
Cardiofaciocutaneous syndrome (Orphanet:1340)
Catel-Manzke syndrome (Orphanet:1388)
Cerebro-facio-thoracic dysplasia (Orphanet:1394)
Classical homocystinuria (Orphanet:394)
Coffin-Lowry syndrome (Orphanet:192)
Coffin-Siris syndrome (Orphanet:1465)
Complete androgen insensitivity syndrome (Orphanet:99429)
Congenital ichthyosis - intellectual deficit - spastic quadriplegia (Orphanet:352333)
Cornelia de Lange syndrome (Orphanet:199)
Cranioectodermal dysplasia 2 (OMIM:613610)
Craniofacial dysplasia-osteopenia syndrome (Orphanet:314555)
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)
Dermato-cardio-skeletal syndrome, Borrone type (Orphanet:1266)
Diaphanospondylodysostosis (Orphanet:66637)
Dislocation of the hip - dysmorphism (Orphanet:2412)
Dubowitz syndrome (Orphanet:235)
ECTODERMAL DYSPLASIA, SENSORINEURAL HEARING LOSS, AND DISTINCTIVEFACIAL FEATURES (OMIM:609944)
EEC syndrome (Orphanet:1896)
EHLERS-DANLOS SYNDROME, BEASLEY-COHEN TYPE (OMIM:608763)
EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE 2 (OMIM:615539)
Ehlers-Danlos syndrome type 1 (Orphanet:90309)
Ehlers-Danlos syndrome, cardiac valvular type (Orphanet:230851)
Ehlers-Danlos syndrome, classic type (Orphanet:287)
Ehlers-Danlos syndrome, dermatosparaxis type (Orphanet:1901)
Ehlers-Danlos syndrome, kyphoscoliotic and deafness type (Orphanet:300179)
Ehlers-Danlos syndrome, kyphoscoliotic type (Orphanet:1900)
Ehlers-Danlos syndrome, vascular type (Orphanet:286)
Emanuel syndrome (Orphanet:96170)
Faciocardiorenal syndrome (Orphanet:1973)
Femoral-facial syndrome (Orphanet:1988)
Floating-Harbor syndrome (Orphanet:2044)
Focal dermal hypoplasia (Orphanet:2092)
Freeman-Sheldon syndrome (Orphanet:2053)
GM1 gangliosidosis (Orphanet:354)
GM1 gangliosidosis type 1 (Orphanet:79255)
Greig cephalopolysyndactyly syndrome (Orphanet:380)
HAJDU-CHENEY SYNDROME (OMIM:102500)
HERNIA, DOUBLE INGUINAL (OMIM:142350)
HUNTER-MACDONALD SYNDROME (OMIM:611962)
HYPEREKPLEXIA, HEREDITARY 1 (OMIM:149400)
Hereditary hyperekplexia (Orphanet:3197)
Hirschsprung disease - nail hypoplasia - dysmorphism (Orphanet:2153)
Hurler syndrome (Orphanet:93473)
Hurler-Scheie syndrome (Orphanet:93476)
Ichthyosis follicularis - alopecia - photophobia (Orphanet:2273)
Insulin-resistance syndrome type A (Orphanet:2297)
Intellectual deficit, X-linked - dysmorphism - cerebral atrophy (Orphanet:2958)
Isolated sedoheptulokinase deficiency (ORPHA:440713)
KAGAMI-OGATA SYNDROME (OMIM:608149)
Kniest dysplasia (Orphanet:485)
LACTIC ACIDURIA DUE TO D-LACTIC ACID (OMIM:245450)
LOEYS-DIETZ SYNDROME 2 (OMIM:610168)
LOEYS-DIETZ SYNDROME 4 (OMIM:614816)
LOEYS-DIETZ SYNDROME, TYPE 2A (OMIM:608967)
Lambert syndrome (Orphanet:1296)
Larsen-like syndrome, B3GAT3 type (Orphanet:284139)
Lateral meningocele syndrome (Orphanet:2789)
Lenz-Majewski hyperostotic dwarfism (Orphanet:2658)
Leprechaunism (Orphanet:508)
MICROPHTHALMIA, SYNDROMIC 9 (OMIM:601186)
MICROSPHEROPHAKIA WITH HERNIA (OMIM:157150)
Marden-Walker syndrome (Orphanet:2461)
Marfan syndrome type 2 (Orphanet:284973)
Marfanoid syndrome, De Silva type (Orphanet:2464)
Matthew-Wood syndrome (Orphanet:2470)
Menkes disease (Orphanet:565)
Methylmalonic acidemia with homocystinuria, type cblJ (Orphanet:369955)
Miller-Dieker syndrome (Orphanet:531)
Mitochondrial encephalo-cardio-myopathy due to TMEM70 deficiency (Orphanet:1194)
Monosomy 18q (Orphanet:1600)
Monosomy 5p (Orphanet:281)
Monosomy 9p (Orphanet:261112)
Mowat-Wilson syndrome (Orphanet:2152)
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 4A (Orphanet:309297)
Mucopolysaccharidosis type 4B (Orphanet:309310)
Mucopolysaccharidosis type 6 (Orphanet:583)
Mucopolysaccharidosis type 7 (Orphanet:584)
Mullerian derivatives - lymphangiectasia - polydactyly (Orphanet:1655)
Multiple epiphyseal dysplasia, Al-Gazali type (Orphanet:166024)
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia (Orphanet:363972)
OMPHALOCELE, AUTOSOMAL (OMIM:164750)
OPITZ-KAVEGGIA SYNDROME (OMIM:305450)
OSTEOGENESIS IMPERFECTA, TYPE VIII (OMIM:610915)
OSTEOGENESIS IMPERFECTA, TYPE X (OMIM:613848)
OTOFACIOOSSEOUS-GONADAL SYNDROME (OMIM:601976)
Omphalocele (Orphanet:660)
Opitz G/BBB syndrome (Orphanet:2745)
Osteoglophonic dwarfism (Orphanet:2645)
PYCR1-related DeBarsy syndrome (Orphanet:293633)
Pancreatic hypoplasia - diabetes - congenital heart disease (Orphanet:2255)
Persistent Müllerian duct syndrome (Orphanet:2856)
Premature ageing appearance-developmental delay-cardiac arrhythmia syndrome (Orphanet:276432)
Pseudoaminopterin syndrome (Orphanet:221120)
Pyruvate dehydrogenase E1-alpha deficiency (Orphanet:79243)
RHINY (OMIM:180360)
RIENHOFF SYNDROME (OMIM:615582)
Rudiger syndrome (Orphanet:3118)
Ruvalcaba syndrome (Orphanet:3121)
SCARF syndrome (Orphanet:3134)
SENER SYNDROME (OMIM:606156)
SHORT syndrome (Orphanet:3163)
SIMOSA CRANIOFACIAL SYNDROME (OMIM:182150)
SKELETAL DYSPLASIA AND PROGRESSIVE CENTRAL NERVOUS SYSTEM DEGENERATION,LETHAL (OMIM:602613)
Scheie syndrome (Orphanet:93474)
Schwartz-Jampel syndrome (Orphanet:800)
Short rib-polydactyly syndrome, Beemer-Langer type (Orphanet:93268)
Short-rib thoracic dysplasia 5 with or without polydactyly (OMIM:614376)
Shprintzen-Goldberg syndrome (Orphanet:2462)
Sialidosis type 1 (Orphanet:812)
Sialuria (Orphanet:3166)
Simpson-Golabi-Behmel syndrome (Orphanet:373)
Simpson-Golabi-Behmel syndrome type 2 (Orphanet:79022)
Spondylocostal dysostosis - anal and genitourinary malformations (Orphanet:94095)
Spondyloepimetaphyseal dysplasia congenita, Strudwick type (Orphanet:93346)
Steinert myotonic dystrophy (Orphanet:273)
Tel Hashomer camptodactyly syndrome (Orphanet:3292)
Tetrasomy 12p (Orphanet:884)
Trigonocephaly - short stature - developmental delay (Orphanet:3369)
Ulnar-mammary syndrome (Orphanet:3138)
VELOCARDIOFACIAL SYNDROME (OMIM:192430)
WHISTLING FACE SYNDROME, RECESSIVE FORM (OMIM:277720)
WIDOW'S PEAK SYNDROME (OMIM:314570)
Weaver syndrome (Orphanet:3447)
Williams syndrome (Orphanet:904)
Wrinkly skin syndrome (Orphanet:2834)
X-linked distal arthrogryposis multiplex congenita (Orphanet:1145)
X-linked reticulate pigmentary disorder with systemic manifestations (Orphanet:85453)