Long nose
Symptom Information:
Symptom ID: | HPO:0003189 | ||||||
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) Abnormal nasal morphology(HPO:0005105) Long nose(HPO:0003189) MedDRA: |
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Database Frequency: | 20 / 7739 | ||||||
Resource: |
All diseases associated with this symptom:
2q32q33 microdeletion syndrome | (Orphanet:251019) |
AREDYLD syndrome | (Orphanet:1133) |
Alagille syndrome due to 20p12 microdeletion | (Orphanet:261600) |
Christianson syndrome | (Orphanet:85278) |
Developmental delay-microcephaly-facial dysmorphism syndrome, Hutterite type | (Orphanet:363444) |
Glomerulonephritis - sparse hair - telangiectasis | (Orphanet:2087) |
Harrod syndrome | (Orphanet:2115) |
LUJAN-FRYNS SYNDROME | (OMIM:309520) |
MENTAL RETARDATION, AUTOSOMAL DOMINANT 27 | (OMIM:615866) |
MOVED TO 210600 | (OMIM:608664) |
Neonatal hemochromatosis | (Orphanet:446) |
Nijmegen breakage syndrome | (Orphanet:647) |
OCULODENTODIGITAL DYSPLASIA, AUTOSOMAL RECESSIVE | (OMIM:257850) |
ROBINOW-SORAUF SYNDROME | (OMIM:180750) |
SIMOSA CRANIOFACIAL SYNDROME | (OMIM:182150) |
SPASTIC PARAPLEGIA 51, AUTOSOMAL RECESSIVE | (OMIM:613744) |
Saethre-Chotzen syndrome | (Orphanet:794) |
Schilbach-Rott syndrome | (Orphanet:2353) |
Stapes ankylosis with broad thumbs and toes | (Orphanet:140917) |
X-linked intellectual deficit - cerebellar hypoplasia | (Orphanet:137831) |