Broad nasal tip

Symptom Information:

Symptom ID: HPO:0000455
Synonyms:
Nasal tip, wide [HPO:0000455]
BROAD UPTURNED NOSE [HPO:0000455]
Broad, upturned nose [HPO:0000455]
Nasal tip, broad [HPO:0000455]
Bulbous nose [Orphanet:8060]
Broad nasal tip [OMIM:Broad nasal tip]
Broad upturned nose [OMIM:Broad upturned nose]
Broad, upturned nose [OMIM:Broad, upturned nose]
Long/large/bulbous nose [Orphanet:8060]
Bulbous nose (in one family) [OMIM:Bulbous nose (in one family)]
Wide nasal tip [OMIM:Wide nasal tip]
Quality:
Cross references:
HPO:0000414 "Bulbous nose" [Orphanet:8060]
Orphanet:8060 "Long/large/bulbous nose" [Orphanet:8060]
OMIM: "Broad nasal tip" [OMIM:Broad nasal tip]
OMIM: "Broad upturned nose" [OMIM:Broad upturned nose]
OMIM: "Broad, upturned nose" [OMIM:Broad, upturned nose]
OMIM: "Bulbous nose (in one family)" [OMIM:Bulbous nose (in one family)]
OMIM: "Wide nasal tip" [OMIM:Wide nasal tip]
Is a (Direct Parents):
HPO         Anteverted nares
HPO         Abnormality of the nasal tip
Orphanet Bulbous nose
Orphanet Abnormality of the nose
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 nares(HPO:0005288)
                      Anteverted nares(HPO:0000463)
                         Broad nasal tip(HPO:0000455)
                   Abnormality of the external nose(HPO:0010938)
                      Abnormality of the nasal tip(HPO:0000436)
                         Broad nasal tip(HPO:0000455)
                      Abnormality of the nasal alae(HPO:0000429)
                         Anteverted nares(HPO:0000463)
                            Broad nasal tip(HPO:0000455)
                   Abnormal nasal morphology(HPO:0005105)
                      Anteverted nares(HPO:0000463)
                         Broad nasal tip(HPO:0000455)
MedDRA:
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)