Inguinal hernia
Symptom Information:
Symptom ID: | HPO:0000023 | |||||||||||||||||||||||||||||||||||
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 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) |
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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) |