Anteriorly placed anus
Symptom Information:
Symptom ID: | HPO:0001545 | |||||||||
Synonyms: |
|
|||||||||
Quality: | ||||||||||
Cross references: |
|
|||||||||
Is a (Direct Parents): |
|
|||||||||
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) |