Thick nasal alae

Symptom Information:

Symptom ID: HPO:0009928
Synonyms:
Ala nasi, thick [HPO:0009928]
Thickening of the alae nasi [HPO:0009928]
Thick ala nasi [Orphanet:8510]
Flared/thick ala nasi [Orphanet:8510]
Quality:
Cross references:
Orphanet:8510 "Flared/thick ala nasi" [Orphanet:8510]
Is a (Direct Parents):
Orphanet Abnormality of the nose
HPO         Abnormality of the nasal alae
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:
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)