Narrow nasal ridge
Symptom Information:
Symptom ID: | HPO:0000418 | |||||
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 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 dorsum(HPO:0011119) Narrow nasal ridge(HPO:0000418) MedDRA: |
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Database Frequency: | 15 / 7739 | |||||
Resource: |
All diseases associated with this symptom:
ALDH18A1-related De Barsy syndrome | (Orphanet:35664) |
Autosomal recessive cutis laxa type 2B | (Orphanet:357064) |
Bazex-Dupré-Christol syndrome | (Orphanet:113) |
CHROMOSOME 22q13 DUPLICATION SYNDROME | (OMIM:615538) |
De Barsy syndrome | (Orphanet:2962) |
Galloway-Mowat syndrome | (Orphanet:2065) |
Intellectual deficit - sparse hair - brachydactyly | (Orphanet:3051) |
Large congenital melanocytic nevus | (Orphanet:626) |
Lethal restrictive dermopathy | (Orphanet:1662) |
Mandibuloacral dysplasia | (Orphanet:2457) |
Mandibuloacral dysplasia with type A lipodystrophy | (Orphanet:90153) |
Mandibuloacral dysplasia with type B lipodystrophy | (Orphanet:90154) |
Microcephalic osteodysplastic dysplasia, Saul-Wilson type | (Orphanet:85172) |
PYCR1-related DeBarsy syndrome | (Orphanet:293633) |
Wiedemann-Rautenstrauch syndrome | (Orphanet:3455) |