Abnormality of the anus

Symptom Information:

Symptom ID: HPO:0004378
Synonyms:
Anorectal anomaly [Orphanet:26760]
Anorectal anomaly (disorder) [Orphanet:26760]
Anus/rectum anomalies [Orphanet:26760]
Anorectal anomalies (in some patients) [OMIM:Anorectal anomalies (in some patients)]
Quality:
Cross references:
Orphanet:26760 "Anus/rectum anomalies" [Orphanet:26760]
OMIM: "Anorectal anomalies (in some patients)" [OMIM:Anorectal anomalies (in some patients)]
UMLS:C2974527 "Anorectal anomaly" [Orphanet:26760]
Is a (Direct Parents):
HPO         Abnormality of the gastrointestinal tract
Orphanet Structural anomalies of the digestive tract
HPO         Anal canal neoplasm
HPO         Anal margin neoplasm
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:
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)