Anal stenosis

Symptom Information:

Symptom ID: HPO:0002025
Synonyms:
Anal stenosis [OMIM:Anal stenosis]
Anal stenosis [MedDRA:10002176]
Anal stricture [MedDRA:10002176]
Anal stenosis (rare, in males) [OMIM:Anal stenosis (rare, in males)]
Anal stricture [OMIM:Anal stricture]
Quality:
Cross references:
OMIM: "Anal stenosis" [OMIM:Anal stenosis]
OMIM: "Anal stenosis (rare, in males)" [OMIM:Anal stenosis (rare, in males)]
OMIM: "Anal stricture" [OMIM:Anal stricture]
Is a (Direct Parents):
MedDRA Anal and rectal stenosis and obstruction
HPO         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)
                   Anal stenosis(HPO:0002025)
MedDRA:
Gastrointestinal disorders(MedDRA:10017947)
    Gastrointestinal stenosis and obstruction(MedDRA:10018008)
       Anal and rectal stenosis and obstruction(MedDRA:10002117)
          Anal stenosis(HPO:0002025)
Database Frequency: 23 / 7739
Resource:

All diseases associated with this symptom:

AXENFELD-RIEGER SYNDROME, TYPE 1 (OMIM:180500)
AXENFELD-RIEGER SYNDROME, TYPE 2 (OMIM:601499)
Acro-renal-ocular syndrome (Orphanet:959)
Axenfeld-Rieger syndrome (Orphanet:782)
Bartsocas-Papas syndrome (Orphanet:1234)
CHARGE syndrome (Orphanet:138)
Currarino triad (Orphanet:1552)
Curry-Jones syndrome (Orphanet:1553)
Diabetic embryopathy (Orphanet:1926)
HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 2 (OMIM:614749)
KABUKI SYNDROME 1 (OMIM:147920)
Kabuki syndrome (Orphanet:2322)
Microcephaly-cardiomyopathy syndrome (Orphanet:2515)
Multiple congenital anomalies - hypotonia - seizures syndrome (Orphanet:280633)
Nijmegen breakage syndrome (Orphanet:647)
OPITZ-KAVEGGIA SYNDROME (OMIM:305450)
Oculotrichoanal syndrome (Orphanet:2717)
Okihiro syndrome (Orphanet:93293)
Opitz G/BBB syndrome (Orphanet:2745)
Osteopathia striata - cranial sclerosis (Orphanet:2780)
Tetrasomy 12p (Orphanet:884)
Townes-Brocks syndrome (Orphanet:857)
Ulnar-mammary syndrome (Orphanet:3138)