Stenosis of the external auditory canal

Symptom Information:

Symptom ID: HPO:0000402
Synonyms:
External auditory canal stenosis [HPO:0000402]
Narrow auditory canals [HPO:0000402]
Narrow external auditory canals [HPO:0000402]
Narrow external auditory meatus [HPO:0000402]
Stenotic external auditory canal [HPO:0000402]
External auditory canal atresia [Orphanet:13440]
Congenital atresia of external auditory canal (disorder) [Orphanet:13440]
Stenosis of external auditory canal (disorder) [Orphanet:13440]
Absence of ear canal (finding) [Orphanet:13440]
Congenital atresia of external auditory canal [Orphanet:13440]
Stenosis of external auditory canal [Orphanet:13440]
Absence of ear canal [Orphanet:13440]
External auditory canal stenosis [OMIM:External auditory canal stenosis]
Narrow auditory canals [OMIM:Narrow auditory canals]
Narrow external auditory canals [OMIM:Narrow external auditory canals]
Narrow external auditory meatus [OMIM:Narrow external auditory meatus]
Stenotic external auditory canal [OMIM:Stenotic external auditory canal]
External auditory canal atresia/stenosis/agenesis [Orphanet:13440]
Ear canal stenosis [Orphanet:13440]
External auditory canal atresia [MedDRA:10054875]
Ear canal stenosis [MedDRA:10061829]
Acquired stenosis of external ear canal [MedDRA:10061829]
Acquired stenosis of external ear canal secondary to inflammation [MedDRA:10061829]
Acquired stenosis of external ear canal, unspecified as to cause [MedDRA:10061829]
Ear canal stenosis NOS [MedDRA:10061829]
Narrow auditory canal [OMIM:Narrow auditory canal]
Narrowed auditory canal [OMIM:Narrowed auditory canal]
Stenotic external auditory canals [OMIM:Stenotic external auditory canals]
Quality:
Cross references:
HPO:0011386 "Narrow internal auditory canal" [Orphanet:13440]
HPO:0011385 "Absent internal auditory canal" [Orphanet:13440]
HPO:0000413 "Atresia of the external auditory canal" [Orphanet:13440]
Orphanet:13440 "External auditory canal atresia/stenosis/agenesis" [Orphanet:13440]
OMIM: "External auditory canal stenosis" [OMIM:External auditory canal stenosis]
OMIM: "Narrow auditory canals" [OMIM:Narrow auditory canals]
OMIM: "Narrow external auditory canals" [OMIM:Narrow external auditory canals]
OMIM: "Narrow external auditory meatus" [OMIM:Narrow external auditory meatus]
OMIM: "Stenotic external auditory canal" [OMIM:Stenotic external auditory canal]
OMIM: "Narrow auditory canal" [OMIM:Narrow auditory canal]
OMIM: "Narrowed auditory canal" [OMIM:Narrowed auditory canal]
OMIM: "Stenotic external auditory canals" [OMIM:Stenotic external auditory canals]
UMLS:C0266597 "Congenital atresia of external auditory canal" [Orphanet:13440]
UMLS:C0395837 "Stenosis of external auditory canal" [Orphanet:13440]
UMLS:C0423488 "Absence of ear canal" [Orphanet:13440]
Is a (Direct Parents):
HPO         Abnormality of the auditory canal
MedDRA External ear disorders NEC
HPO         Cutaneous stenosis of the external auditory canal
HPO         Osseous stenosis of the external auditory canal
Orphanet Abnormality of the outer ear
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the ear(HPO:0000598)
          Abnormality of the outer ear(HPO:0000356)
             Abnormality of the auditory canal(HPO:0000372)
                Stenosis of the external auditory canal(HPO:0000402)
MedDRA:
Ear and labyrinth disorders(MedDRA:10013993)
    External ear disorders (excl congenital)(MedDRA:10015732)
       External ear disorders NEC(MedDRA:10027672)
          Stenosis of the external auditory canal(HPO:0000402)
Database Frequency: 22 / 7739
Resource:

All diseases associated with this symptom:

ANTERIOR CHAMBER CLEAVAGE DISORDER, CEREBELLAR HYPOPLASIA, HYPOTHYROIDISM,AND TRACHEAL STENOSIS (OMIM:601427)
AURICULOCONDYLAR SYNDROME 3 (OMIM:615706)
Antley-Bixler syndrome (Orphanet:83)
Auriculocondylar syndrome (Orphanet:137888)
BOR syndrome (Orphanet:107)
Blepharophimosis-intellectual deficit syndrome, Ohdo type (Orphanet:2728)
CRANIOSYNOSTOSIS-MENTAL RETARDATION SYNDROME OF LIN AND GETTIG (OMIM:218649)
Cat-eye syndrome (Orphanet:195)
DIAMOND-BLACKFAN ANEMIA 11 (OMIM:614900)
Dysmorphism - conductive hearing loss - heart defect (Orphanet:289553)
External auditory canal aplasia/hypoplasia (Orphanet:141074)
Focal dermal hypoplasia (Orphanet:2092)
MANDIBULOFACIAL DYSOSTOSIS WITH PTOSIS, AUTOSOMAL DOMINANT (OMIM:608257)
Monosomy 18q (Orphanet:1600)
Monosomy 5p (Orphanet:281)
OSTEOPETROSIS, AUTOSOMAL RECESSIVE 8 (OMIM:615085)
Peters-plus syndrome (Orphanet:709)
Phocomelia - ectrodactyly - deafness - sinus arrhythmia (Orphanet:2878)
SKELETAL DYSPLASIA AND PROGRESSIVE CENTRAL NERVOUS SYSTEM DEGENERATION,LETHAL (OMIM:602613)
Tetrasomy 12p (Orphanet:884)
Wolf-Hirschhorn syndrome (Orphanet:280)
Zechi-Ceide syndrome (Orphanet:217017)