Anteriorly placed anus

Symptom Information:

Symptom ID: HPO:0001545
Synonyms:
Anteriorly displaced anus [HPO:0001545]
Anus anteposition [HPO:0001545]
Anus anteposition [Orphanet:26800]
Anus malposition [Orphanet:26800]
Anteriorly displaced anus [OMIM:Anteriorly displaced anus]
Anteriorly placed anus [OMIM:Anteriorly placed anus]
Anus ectopia/anteposition/malposition [Orphanet:26800]
Anteriorly displaced anus (in some patients) [OMIM:Anteriorly displaced anus (in some patients)]
Anteriorly places anus [OMIM:Anteriorly places anus]
Quality:
Cross references:
HPO:0004397 "Ectopic anus" [Orphanet:26800]
Orphanet:26800 "Anus ectopia/anteposition/malposition" [Orphanet:26800]
OMIM: "Anteriorly displaced anus" [OMIM:Anteriorly displaced anus]
OMIM: "Anteriorly placed anus" [OMIM:Anteriorly placed anus]
OMIM: "Anteriorly displaced anus (in some patients)" [OMIM:Anteriorly displaced anus (in some patients)]
OMIM: "Anteriorly places anus" [OMIM:Anteriorly places anus]
Is a (Direct Parents):
HPO         Ectopic anus
Orphanet Abnormality of the anus
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)
                   Ectopic anus(HPO:0004397)
                      Anteriorly placed anus(HPO:0001545)
MedDRA:
Database Frequency: 55 / 7739
Resource:

All diseases associated with this symptom:

1p36 deletion syndrome (Orphanet:1606)
3C syndrome (Orphanet:7)
3q29 microduplication (Orphanet:251038)
ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS (OMIM:201750)
Apert syndrome (Orphanet:87)
Atrioventricular defect - blepharophimosis -radial defects (Orphanet:1352)
Autosomal dominant Robinow syndrome (Orphanet:3107)
Autosomal recessive Robinow syndrome (Orphanet:1507)
BNAR syndrome (Orphanet:217266)
Baller-Gerold syndrome (Orphanet:1225)
Bladder exstrophy (Orphanet:93930)
Cerebro-facio-articular syndrome (Orphanet:314679)
Cloacal exstrophy (Orphanet:93929)
Cooper-Jabs syndrome (Orphanet:1488)
Craniosynostosis - anal anomalies - porokeratosis (Orphanet:85199)
Cutis gyrata - acanthosis nigricans - craniosynostosis (Orphanet:1555)
Cutis laxa (Orphanet:209)
Distal monosomy 10p (Orphanet:1580)
Exstrophy-epispadias complex (Orphanet:322)
Familial caudal dysgenesis (Orphanet:1768)
Focal dermal hypoplasia (Orphanet:2092)
Fraser syndrome (Orphanet:2052)
Fryns syndrome (Orphanet:2059)
HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 1 (OMIM:239300)
Hyperphosphatasia-intellectual deficiency syndrome (Orphanet:247262)
Isolated Klippel-Feil syndrome (Orphanet:2345)
Jacobsen syndrome (Orphanet:2308)
Johanson-Blizzard syndrome (Orphanet:2315)
Juberg-Hayward syndrome (Orphanet:2319)
Lenz-Majewski hyperostotic dwarfism (Orphanet:2658)
Limb body wall complex (Orphanet:2369)
MICROPHTHALMIA, SYNDROMIC 7 (OMIM:309801)
MITCHELL-RILEY SYNDROME (OMIM:615710)
McKusick-Kaufman syndrome (Orphanet:2473)
Medeira-Dennis-Donnai syndrome (Orphanet:2476)
Mosaic trisomy 14 (Orphanet:1703)
OPITZ-KAVEGGIA SYNDROME (OMIM:305450)
Oculoauriculovertebral spectrum with radial defects (Orphanet:2549)
Oculotrichoanal syndrome (Orphanet:2717)
PELVIS syndrome (Orphanet:83628)
Renal-genital-middle ear anomalies (Orphanet:1092)
Rothmund-Thomson syndrome (Orphanet:2909)
SENER SYNDROME (OMIM:606156)
Severe intellectual deficit - epilepsy - anal anomalies - distal phalangeal hypoplasia (Orphanet:94066)
Short rib-polydactyly syndrome, Verma-Naumoff type (Orphanet:93271)
Short stature - craniofacial anomalies - genital hypoplasia (Orphanet:2994)
Short stature - deafness - neutrophil dysfunction - dysmorphism (Orphanet:2866)
Tetrasomy 12p (Orphanet:884)
Thrombocytopenia - Robin sequence (Orphanet:3323)
Toriello-Carey syndrome (Orphanet:3338)
Townes-Brocks syndrome (Orphanet:857)
Trisomy 20p (Orphanet:261318)
Ulnar-mammary syndrome (Orphanet:3138)
VAN MALDERGEM SYNDROME 1 (OMIM:601390)
Xp22.3 microdeletion syndrome (Orphanet:1643)