Stenosis of the external auditory canal
Symptom Information:
Symptom ID: | HPO:0000402 | ||||||||||||||||||||||||||||
Synonyms: |
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Is a (Direct Parents): | |||||||||||||||||||||||||||||
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) |
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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) |