Hernia of the abdominal wall
Symptom Information:
Symptom ID: | HPO:0004299 | |||||||||||||||||||||||||||||
Synonyms: |
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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) 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) MedDRA: 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) |
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Database Frequency: | 176 / 7739 | |||||||||||||||||||||||||||||
Resource: |
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) |
OMPHALOCELE, AUTOSOMAL | (OMIM:164750) |
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) |