Atresia of the external auditory canal
Symptom Information:
Symptom ID: | HPO:0000413 | |||||||||||||||||||||||||||||||||||||||||
Synonyms: |
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Cross references: |
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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) Atresia of the external auditory canal(HPO:0000413) MedDRA: Ear and labyrinth disorders(MedDRA:10013993) External ear disorders (excl congenital)(MedDRA:10015732) External ear disorders NEC(MedDRA:10027672) Atresia of the external auditory canal(HPO:0000413) |
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Database Frequency: | 32 / 7739 | |||||||||||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
AURAL ATRESIA, CONGENITAL | (OMIM:607842) |
Acro-oto-ocular syndrome | (Orphanet:2980) |
Ankyloblepharon - ectodermal defects - cleft lip/palate | (Orphanet:1071) |
Branchiogenic deafness syndrome | (Orphanet:50815) |
Cerebro-facio-articular syndrome | (Orphanet:314679) |
Conductive deafness - ptosis - skeletal anomalies | (Orphanet:3236) |
Cooper-Jabs syndrome | (Orphanet:1488) |
Crouzon disease | (Orphanet:207) |
DIAMOND-BLACKFAN ANEMIA 10 | (OMIM:613309) |
DIAMOND-BLACKFAN ANEMIA 11 | (OMIM:614900) |
EXTERNAL AUDITORY CANAL, BILATERAL ATRESIA OF, WITH CONGENITAL VERTICALTALUS | (OMIM:133705) |
Ear-patella-short stature syndrome | (Orphanet:2554) |
External auditory canal aplasia/hypoplasia | (Orphanet:141074) |
Fraser syndrome | (Orphanet:2052) |
Goldenhar syndrome | (Orphanet:374) |
Hypertelorism-microtia-facial clefting syndrome | (Orphanet:2213) |
LAMBOTTE SYNDROME | (OMIM:245552) |
LETHAL SHORT-LIMB SKELETAL DYSPLASIA, AL GAZALI TYPE | (OMIM:601356) |
MANDIBULOFACIAL DYSOSTOSIS WITH PTOSIS, AUTOSOMAL DOMINANT | (OMIM:608257) |
MEIER-GORLIN SYNDROME 1 | (OMIM:224690) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 1 | (OMIM:236670) |
Mandibulofacial dysostosis-microcephaly syndrome | (Orphanet:79113) |
Monosomy 18q | (Orphanet:1600) |
Muscle-eye-brain disease | (Orphanet:588) |
Nager syndrome | (Orphanet:245) |
Neuroectodermal syndrome, Johnson type | (Orphanet:2316) |
Oculoauriculovertebral spectrum with radial defects | (Orphanet:2549) |
Pallister-Hall syndrome | (Orphanet:672) |
SHORT STATURE, AUDITORY CANAL ATRESIA, MANDIBULAR HYPOPLASIA, ANDSKELETAL ABNORMALITIES | (OMIM:602471) |
VAN MALDERGEM SYNDROME 1 | (OMIM:601390) |
VAN MALDERGEM SYNDROME 2 | (OMIM:615546) |
Wilson-Turner syndrome | (Orphanet:3459) |