Broad nasal tip
Symptom Information:
Symptom ID: | HPO:0000455 | |||||||||||
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 alae(HPO:0000429) Anteverted nares(HPO:0000463) Broad nasal tip(HPO:0000455) Abnormality of the nasal tip(HPO:0000436) Broad nasal tip(HPO:0000455) Abnormal nasal morphology(HPO:0005105) Anteverted nares(HPO:0000463) Broad nasal tip(HPO:0000455) Abnormality of the nares(HPO:0005288) Anteverted nares(HPO:0000463) Broad nasal tip(HPO:0000455) MedDRA: |
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Database Frequency: | 67 / 7739 | |||||||||||
Resource: |
All diseases associated with this symptom:
2q37 microdeletion syndrome | (Orphanet:1001) |
ACRODYSOSTOSIS 1 WITH OR WITHOUT HORMONE RESISTANCE | (OMIM:101800) |
AREDYLD syndrome | (Orphanet:1133) |
Acrodysostosis with multiple hormone resistance | (Orphanet:280651) |
Acromelic frontonasal dysplasia | (Orphanet:1827) |
Atkin-Flaitz syndrome | (Orphanet:1193) |
Autosomal recessive distal osteolysis syndrome | (Orphanet:2776) |
BREASTS AND/OR NIPPLES, APLASIA OR HYPOPLASIA OF, 2 | (OMIM:616001) |
Branchio-oculo-facial syndrome | (Orphanet:1297) |
CHROMOSOME 6q11-q14 DELETION SYNDROMECHROMOSOME 6q13-q14 DELETION SYNDROME, INCLUDED | (OMIM:613544) |
CLARK-BARAITSER SYNDROME | (OMIM:300602) |
COFFIN-SIRIS SYNDROME | (OMIM:135900) |
CORNELIA DE LANGE SYNDROME 5 | (OMIM:300882) |
Cardiodysrhythmic potassium-sensitive periodic paralysis | (Orphanet:37553) |
Cataract - intellectual deficit - hypogonadism | (Orphanet:1387) |
Char syndrome | (Orphanet:46627) |
Coffin-Siris syndrome | (Orphanet:1465) |
Donnai-Barrow syndrome | (Orphanet:2143) |
Dubowitz syndrome | (Orphanet:235) |
EEC syndrome | (Orphanet:1896) |
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 23 | (OMIM:615859) |
Focal dermal hypoplasia | (Orphanet:2092) |
Frank-Ter Haar syndrome | (Orphanet:137834) |
Frontonasal dysplasia | (Orphanet:250) |
Glycogen storage disease due to glycogen debranching enzyme deficiency | (Orphanet:366) |
HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 1 | (OMIM:239300) |
HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 2 | (OMIM:614749) |
HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 4 | (OMIM:615716) |
HYPERTRICHOSIS, HYPERKERATOSIS, MENTAL RETARDATION, AND DISTINCTIVEFACIAL FEATURES | (OMIM:609943) |
Hurler syndrome | (Orphanet:93473) |
Hydrocephalus - costovertebral dysplasia - Sprengel anomaly | (Orphanet:2180) |
Hyperphosphatasia-intellectual deficiency syndrome | (Orphanet:247262) |
Hypertelorism-microtia-facial clefting syndrome | (Orphanet:2213) |
Joubert syndrome with orofaciodigital defect | (Orphanet:2754) |
KABUKI SYNDROME 2 | (OMIM:300867) |
Large congenital melanocytic nevus | (Orphanet:626) |
Leprechaunism | (Orphanet:508) |
Lymphedema - atrial septal defects - facial changes | (Orphanet:86915) |
MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND WITH OR WITHOUT AUTISTICFEATURES | (OMIM:613670) |
MENTAL RETARDATION WITH OPTIC ATROPHY, FACIAL DYSMORPHISM, MICROCEPHALY,AND SHORT STATURE | (OMIM:609037) |
MENTAL RETARDATION, AUTOSOMAL DOMINANT 18 | (OMIM:615074) |
MENTAL RETARDATION, AUTOSOMAL DOMINANT 32 | (OMIM:616268) |
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 41 | (OMIM:615637) |
MENTAL RETARDATION, X-LINKED 19 | (OMIM:300844) |
MICROCEPHALY, GROWTH RETARDATION, CATARACT, HEARING LOSS, AND UNUSUALAPPEARANCE | (OMIM:612947) |
MICROPHTHALMIA, SYNDROMIC 12 | (OMIM:615524) |
Mandibulofacial dysostosis - macroblepharon - macrostomia | (Orphanet:357158) |
Microcephaly - lymphedema - chorioretinopathy | (Orphanet:2526) |
Microcornea-myopic chorioretinal atrophy-telecanthus syndrome | (Orphanet:369970) |
Mucopolysaccharidosis type 1 | (Orphanet:579) |
Multiple epiphyseal dysplasia, Lowry type | (Orphanet:166016) |
Neonatal hemochromatosis | (Orphanet:446) |
OROFACIODIGITAL SYNDROME VI | (OMIM:277170) |
Oculofaciocardiodental syndrome | (Orphanet:2712) |
Orofaciodigital syndrome type 2 | (Orphanet:2751) |
Orofaciodigital syndrome type 8 | (Orphanet:2755) |
Orofaciodigital syndrome type 9 | (Orphanet:141007) |
Overgrowth - macrocephaly - facial dysmorphism | (Orphanet:137634) |
Rabson-Mendenhall syndrome | (Orphanet:769) |
SPONDYLOEPIPHYSEAL DYSPLASIA TARDA WITH CHARACTERISTIC FACIES | (OMIM:600093) |
STARGARDT MACULAR DEGENERATION, ABSENT OR HYPOPLASTIC CORPUS CALLOSUM,MENTAL RETARDATION, AND DYSMORPHIC FEATURES | (OMIM:612948) |
Spondylocarpotarsal synostosis | (Orphanet:3275) |
Spondyloepimetaphyseal dysplasia, Bieganski type | (Orphanet:168448) |
W syndrome | (Orphanet:2804) |
Williams syndrome | (Orphanet:904) |
Wilson-Turner syndrome | (Orphanet:3459) |
X-linked intellectual deficit, Najm type | (Orphanet:163937) |