Anotia

Symptom Information:

Symptom ID: HPO:0009892
Synonyms:
Absent ear [HPO:0009892]
ABSENT EARS [HPO:0009892]
Congenital absence of external ear [HPO:0009892]
Absence of ear (finding) [Orphanet:13080]
Congenital absence of external ear (disorder) [Orphanet:13080]
Absence of ear [Orphanet:13080]
Congenital absence of external ear [Orphanet:13080]
Absent ears [OMIM:Absent ears]
Anotia [OMIM:Anotia]
Microtia/cryptomicrotia/anotia/external auditory canal/pinnae aplasia/hypoplasia [Orphanet:13080]
Anotia [Orphanet:13080]
Anotia [MedDRA:10002654]
Absence of ear lobe, congenital [MedDRA:10002654]
Congenital absence of external ear [MedDRA:10002654]
Congenital auricle absence [MedDRA:10002654]
Quality:
Cross references:
Orphanet:13080 "Microtia/cryptomicrotia/anotia/external auditory canal/pinnae aplasia/hypoplasia" [Orphanet:13080]
OMIM: "Absent ears" [OMIM:Absent ears]
OMIM: "Anotia" [OMIM:Anotia]
UMLS:C0702139 "Anotia" [HPO:0009892]
UMLS:C0559900 "Absence of ear" [Orphanet:13080]
UMLS:C0702139 "Congenital absence of external ear" [Orphanet:13080]
Is a (Direct Parents):
HPO         Aplasia/Hypoplasia of the external ear
Orphanet Atresia of the external auditory canal
Orphanet Abnormality of the outer ear
MedDRA External ear disorders congenital
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the ear(HPO:0000598)
          Aplasia/Hypoplasia of the ear(HPO:0008771)
             Aplasia/Hypoplasia of the external ear(HPO:0008772)
                Anotia(HPO:0009892)
          Abnormality of the outer ear(HPO:0000356)
             Aplasia/Hypoplasia of the external ear(HPO:0008772)
                Anotia(HPO:0009892)
MedDRA:
Congenital, familial and genetic disorders(MedDRA:10010331)
    Ear and labyrinthine disorders congenital(MedDRA:10013995)
       External ear disorders congenital(MedDRA:10015733)
          Anotia(HPO:0009892)
Database Frequency: 8 / 7739
Resource:

All diseases associated with this symptom:

Anotia (Orphanet:93976)
COCOON SYNDROME (OMIM:613630)
Diabetic embryopathy (Orphanet:1926)
Goldenhar syndrome (Orphanet:374)
Isotretinoin-like syndrome (Orphanet:2306)
MANDIBULOFACIAL DYSOSTOSIS WITH PTOSIS, AUTOSOMAL DOMINANT (OMIM:608257)
MICROTIA WITH MEATAL ATRESIA AND CONDUCTIVE DEAFNESS (OMIM:251800)
Wilson-Turner syndrome (Orphanet:3459)