Aplasia/Hypoplasia of the earlobes

Symptom Information:

Symptom ID: HPO:0009906
Synonyms:
ABSENT EAR LOBES [HPO:0009906]
Absent ear lobes [OMIM:Absent ear lobes]
Quality:
Cross references:
OMIM: "Absent ear lobes" [OMIM:Absent ear lobes]
Is a (Direct Parents):
HPO         Abnormality of earlobe
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 pinna(HPO:0000377)
                Abnormality of earlobe(HPO:0000363)
                   Aplasia/Hypoplasia of the earlobes(HPO:0009906)
MedDRA:
Database Frequency: 41 / 7739
Resource:

All diseases associated with this symptom:

22q11.2 deletion syndrome (Orphanet:567)
Alpha-thalassemia - intellectual deficit syndrome linked to chromosome 16 (Orphanet:98791)
Anophthalmia plus syndrome (Orphanet:1104)
Auriculoosteodysplasia (Orphanet:114)
Branchiogenic deafness syndrome (Orphanet:50815)
CHARGE syndrome (Orphanet:138)
Camptodactyly syndrome, Guadalajara type 1 (Orphanet:1327)
Cohen syndrome (Orphanet:193)
Cutis gyrata - acanthosis nigricans - craniosynostosis (Orphanet:1555)
Deafness - ear malformation - facial palsy (Orphanet:3232)
Distal monosomy 9p (Orphanet:1642)
Distal trisomy 6p (Orphanet:1745)
EHLERS-DANLOS SYNDROME, PROGEROID TYPE, 1 (OMIM:130070)
Ehlers-Danlos syndrome, vascular type (Orphanet:286)
Flat face - microstomia - ear anomaly (Orphanet:1968)
Hirsutism - skeletal dysplasia - intellectual deficit (Orphanet:2156)
Hydrocephalus - blue sclerae - nephropathy (Orphanet:2186)
Intellectual deficit - polydactyly - uncombable hair (Orphanet:3082)
Intellectual deficit, X-linked - dysmorphism - cerebral atrophy (Orphanet:2958)
Intellectual deficit, X-linked, Vitale type (Orphanet:85289)
Jacobsen syndrome (Orphanet:2308)
Lacrimo-auriculo-dento-digital syndrome (Orphanet:2363)
MENTAL RETARDATION WITH OPTIC ATROPHY, FACIAL DYSMORPHISM, MICROCEPHALY,AND SHORT STATURE (OMIM:609037)
Marfanoid habitus - intellectual deficit, autosomal recessive (Orphanet:2463)
Microcephalic osteodysplastic primordial dwarfism type 2 (Orphanet:2637)
Monosomy 9p (Orphanet:261112)
Non-distal trisomy 13q (Orphanet:1702)
Odontotrichomelic syndrome (Orphanet:2723)
Oliver syndrome (Orphanet:2920)
Oto-onycho-peroneal syndrome (Orphanet:2793)
PHAVER syndrome (Orphanet:2876)
Phocomelia - ectrodactyly - deafness - sinus arrhythmia (Orphanet:2878)
Postaxial polydactyly - dental and vertebral anomalies (Orphanet:2916)
Roberts syndrome (Orphanet:3103)
Scalp-ear-nipple syndrome (Orphanet:2036)
Seckel syndrome (Orphanet:808)
Teebi-Shaltout syndrome (Orphanet:3291)
Urban-Rogers-Meyer syndrome (Orphanet:3409)
Wiedemann-Rautenstrauch syndrome (Orphanet:3455)
Wilson-Turner syndrome (Orphanet:3459)
Yunis-Varon syndrome (Orphanet:3472)