Abnormality of the anus
Symptom Information:
Symptom ID: | HPO:0004378 | ||||||||
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 organs(HPO:0002012) Abnormality of the gastrointestinal tract(HPO:0011024) Abnormality of the anus(HPO:0004378) MedDRA: |
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Database Frequency: | 34 / 7739 | ||||||||
Resource: |
All diseases associated with this symptom:
1p36 deletion syndrome | (Orphanet:1606) |
ANAL SPHINCTER MYOPATHY, INTERNAL | (OMIM:105565) |
Axial mesodermal dysplasia spectrum | (Orphanet:1834) |
Bladder exstrophy | (Orphanet:93930) |
Corpus callosum agenesis - double urinary collecting system | (Orphanet:1492) |
Dubowitz syndrome | (Orphanet:235) |
Dyskeratosis congenita | (Orphanet:1775) |
Dysmorphism - multiple structural anomalies | (Orphanet:1780) |
Dystrophic epidermolysis bullosa | (Orphanet:303) |
Ehlers-Danlos syndrome, hypermobility type | (Orphanet:285) |
Fraser syndrome | (Orphanet:2052) |
HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 1 | (OMIM:239300) |
Hereditary acrokeratotic poikiloderma, Weary type | (Orphanet:2907) |
Hereditary mixed polyposis syndrome | (Orphanet:157794) |
Hereditary mucoepithelial dysplasia | (Orphanet:1839) |
Juvenile hyaline fibromatosis | (Orphanet:2028) |
Juvenile polyposis syndrome | (Orphanet:2929) |
Kindler syndrome | (Orphanet:2908) |
Microphthalmia with linear skin defects syndrome | (Orphanet:2556) |
Monosomy 13q14 | (Orphanet:1587) |
Nijmegen breakage syndrome | (Orphanet:647) |
Oculotrichoanal syndrome | (Orphanet:2717) |
Peutz-Jeghers syndrome | (Orphanet:2869) |
Recessive dystrophic epidermolysis bullosa inversa | (Orphanet:79409) |
Recessive dystrophic epidermolysis bullosa-generalized other | (Orphanet:89842) |
Recombinant 8 syndrome | (Orphanet:96167) |
Rhombencephalosynapsis | (Orphanet:59315) |
Sacrococcygeal dysgenesis association | (Orphanet:1773) |
Scleroderma | (Orphanet:801) |
Severe generalized recessive dystrophic epidermolysis bullosa | (Orphanet:79408) |
Townes-Brocks syndrome | (Orphanet:857) |
VACTERL/VATER association | (Orphanet:887) |
Williams syndrome | (Orphanet:904) |
XK aprosencephaly | (Orphanet:3469) |