Aplasia/Hypoplasia of the earlobes
Symptom Information:
Symptom ID: | HPO:0009906 | ||
Synonyms: |
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Quality: | |||
Cross references: |
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Is a (Direct Parents): |
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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 pinna(HPO:0000377) Abnormality of earlobe(HPO:0000363) Aplasia/Hypoplasia of the earlobes(HPO:0009906) MedDRA: |
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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) |