Thick nasal alae
Symptom Information:
Symptom ID: | HPO:0009928 | ||||
Synonyms: |
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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 head or neck(HPO:0000152) Abnormality of the head(HPO:0000234) Abnormality of the face(HPO:0000271) Abnormality of the nose(HPO:0000366) Abnormality of the external nose(HPO:0010938) Abnormality of the nasal alae(HPO:0000429) Thick nasal alae(HPO:0009928) MedDRA: |
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Database Frequency: | 21 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
15q24 microdeletion syndrome | (Orphanet:94065) |
17q11.2 microduplication syndrome | (Orphanet:139474) |
Acromegaloid facial appearance syndrome | (Orphanet:965) |
Acromelic frontonasal dysplasia | (Orphanet:1827) |
Coffin-Lowry syndrome | (Orphanet:192) |
Deafness - onychodystrophy | (Orphanet:3231) |
GAPO syndrome | (Orphanet:2067) |
Gingival fibromatosis-hypertrichosis syndrome | (Orphanet:2026) |
Intellectual deficit - sparse hair - brachydactyly | (Orphanet:3051) |
Intellectual deficit, X-linked, Stevenson type | (Orphanet:85325) |
Koolen-De Vries syndrome | (Orphanet:96169) |
Langer-Giedion syndrome | (Orphanet:502) |
Leprechaunism | (Orphanet:508) |
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 35 | (OMIM:615162) |
Mucopolysaccharidosis type 1 | (Orphanet:579) |
Mucopolysaccharidosis type 2 | (Orphanet:580) |
Mucopolysaccharidosis type 6 | (Orphanet:583) |
Mullerian derivatives - lymphangiectasia - polydactyly | (Orphanet:1655) |
Proteus syndrome | (Orphanet:744) |
TEMPLE-BARAITSER SYNDROME | (OMIM:611816) |
Trisomy 17p | (Orphanet:261290) |