Aplasia/Hypoplasia of the external ear

Symptom Information:

Symptom ID: HPO:0008772
Cross references:
Is a (Direct Parents):
HPO         Abnormality of the outer ear
HPO         Aplasia/Hypoplasia of the ear
HPO         Focal absence of the external ear
Is a (Whole tree): HPO:
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the ear(HPO:0000598)
          Abnormality of the outer ear(HPO:0000356)
             Aplasia/Hypoplasia of the external ear(HPO:0008772)
          Aplasia/Hypoplasia of the ear(HPO:0008771)
             Aplasia/Hypoplasia of the external ear(HPO:0008772)
Database Frequency: 67 / 7739

All diseases associated with this symptom:

1p36 deletion syndrome (Orphanet:1606)
20p12.3 microdeletion syndrome (Orphanet:261295)
3-hydroxyisobutyric aciduria (Orphanet:939)
Ablepharon macrostomia syndrome (Orphanet:920)
Acro-pectoro-renal dysplasia (Orphanet:956)
Acrofacial dysostosis, Rodriguez type (Orphanet:1788)
Agnathia - holoprosencephaly - situs inversus (Orphanet:990)
Aspartylglucosaminuria (Orphanet:93)
Atrioventricular defect - blepharophimosis -radial defects (Orphanet:1352)
Auriculoosteodysplasia (Orphanet:114)
Axial mesodermal dysplasia spectrum (Orphanet:1834)
Blepharophimosis-intellectual deficit syndrome, Ohdo type (Orphanet:2728)
CHARGE syndrome (Orphanet:138)
Camptodactyly syndrome, Guadalajara type 1 (Orphanet:1327)
Conductive deafness - malformed external ear (Orphanet:3216)
Coxoauricular syndrome (Orphanet:1508)
Craniosynostosis, Herrmann-Opitz type (Orphanet:2145)
Crossed polysyndactyly (Orphanet:2935)
Cryptomicrotia - brachydactyly - excess fingertip arch (Orphanet:1547)
Deafness - ear malformation - facial palsy (Orphanet:3232)
Deafness with labyrinthine aplasia, microtia, and microdontia (Orphanet:90024)
Diabetic embryopathy (Orphanet:1926)
Disorder of sex development - intellectual deficit (Orphanet:2983)
Distal monosomy 17q (Orphanet:1597)
Distal monosomy 9p (Orphanet:1642)
Dysmorphism - short stature - deafness - disorder of sex development (Orphanet:2282)
Ear-patella-short stature syndrome (Orphanet:2554)
Embryofetopathy due to oral anticoagulant therapy (Orphanet:1914)
Familial visceral myopathy (Orphanet:2604)
Femoral-facial syndrome (Orphanet:1988)
Fraser syndrome (Orphanet:2052)
Goldenhar syndrome (Orphanet:374)
Gonadal dysgenesis, XY type - associated anomalies (Orphanet:1770)
Hand-foot-genital syndrome (Orphanet:2438)
Hennekam-Beemer syndrome (Orphanet:2135)
Holoprosencephaly - radial heart renal anomalies (Orphanet:3186)
Hypertelorism-microtia-facial clefting syndrome (Orphanet:2213)
Intellectual deficit - myopathy - short stature - endocrine defect (Orphanet:3068)
Isotretinoin syndrome (Orphanet:2305)
Isotretinoin-like syndrome (Orphanet:2306)
Lambert syndrome (Orphanet:1296)
Lethal restrictive dermopathy (Orphanet:1662)
Microphthalmia - microtia - fetal akinesia (Orphanet:2547)
Microtia - eye coloboma - imperforation of the nasolacrimal duct (Orphanet:139450)
Mosaic trisomy 14 (Orphanet:1703)
Mycophenolate mofetil embryopathy (Orphanet:268249)
Nager syndrome (Orphanet:245)
Neuroectodermal syndrome, Johnson type (Orphanet:2316)
Oculoauriculovertebral spectrum with radial defects (Orphanet:2549)
Orofaciodigital syndrome type 4 (Orphanet:2753)
Patterson-Stevenson-Fontaine syndrome (Orphanet:2439)
Peters-plus syndrome (Orphanet:709)
Phocomelia - ectrodactyly - deafness - sinus arrhythmia (Orphanet:2878)
Pseudoprogeria syndrome (Orphanet:2985)
Saethre-Chotzen syndrome (Orphanet:794)
Scalp-ear-nipple syndrome (Orphanet:2036)
Short stature - craniofacial anomalies - genital hypoplasia (Orphanet:2994)
Teebi-Shaltout syndrome (Orphanet:3291)
Tetraamelia - multiple malformations (Orphanet:3301)
Thalidomide embryopathy (Orphanet:3312)
Townes-Brocks syndrome (Orphanet:857)
Treacher-Collins syndrome (Orphanet:861)
Trisomy 1q (Orphanet:261344)
VACTERL with hydrocephalus (Orphanet:3412)
Verloove Vanhorick-Brubakk syndrome (Orphanet:3429)
Wolf-Hirschhorn syndrome (Orphanet:280)
Yunis-Varon syndrome (Orphanet:3472)