Convex nasal ridge

Symptom Information:

Symptom ID: HPO:0000444
Synonyms:
Beaklike protrusion [HPO:0000444]
Hooked nose [HPO:0000444]
Beaklike protrusion [OMIM:Beaklike protrusion]
Convex nasal ridge [OMIM:Convex nasal ridge]
Hooked nose [OMIM:Hooked nose]
Beaked nose [Orphanet:8270]
Beaked nose [OMIM:Beaked nose]
Beaked nose (in some patients) [OMIM:Beaked nose (in some patients)]
Hooked nose (in some patients) [OMIM:Hooked nose (in some patients)]
Quality:
Cross references:
Orphanet:8270 "Beaked nose" [Orphanet:8270]
OMIM: "Beaklike protrusion" [OMIM:Beaklike protrusion]
OMIM: "Convex nasal ridge" [OMIM:Convex nasal ridge]
OMIM: "Hooked nose" [OMIM:Hooked nose]
OMIM: "Beaked nose" [OMIM:Beaked nose]
OMIM: "Beaked nose (in some patients)" [OMIM:Beaked nose (in some patients)]
OMIM: "Hooked nose (in some patients)" [OMIM:Hooked nose (in some patients)]
Is a (Direct Parents):
Orphanet Abnormality of the nose
HPO         Abnormal nasal morphology
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)
                      Convex nasal ridge(HPO:0000444)
MedDRA:
Database Frequency: 87 / 7739
Resource:

All diseases associated with this symptom:

15q14 microdeletion syndrome (Orphanet:261190)
2q32q33 microdeletion syndrome (Orphanet:251019)
AICARDI-GOUTIERES SYNDROME 4 (OMIM:610333)
ASYMMETRIC SHORT STATURE SYNDROME (OMIM:108450)
Acrogeria (Orphanet:2500)
Alar cartilages hypoplasia - coloboma - telecanthus (Orphanet:2007)
Aortic arch anomaly - peculiar facies - intellectual deficit (Orphanet:1110)
Apert syndrome (Orphanet:87)
Arterial tortuosity syndrome (Orphanet:3342)
Arthrogryposis - renal dysfunction - cholestasis (Orphanet:2697)
BRESEK syndrome (Orphanet:85284)
Bangstad syndrome (Orphanet:1227)
Bird headed-dwarfism, Montreal type (Orphanet:2617)
Bohring-Opitz syndrome (Orphanet:97297)
Brachydactyly - mesomelia - intellectual deficit - heart defects (Orphanet:1277)
CRANIOSYNOSTOSIS WITH OCULAR ABNORMALITIES AND HALLUCAL DEFECTS (OMIM:608279)
CRANIOSYNOSTOSIS-MENTAL RETARDATION-CLEFTING SYNDROME (OMIM:218650)
CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IB (OMIM:614437)
Cartilage-hair hypoplasia (Orphanet:175)
Cenani-Lenz syndrome (Orphanet:3258)
Cernunnos-XLF deficiency (Orphanet:169079)
Cohen syndrome (Orphanet:193)
Craniosynostosis, Herrmann-Opitz type (Orphanet:2145)
Crouzon disease (Orphanet:207)
Crouzon syndrome - acanthosis nigricans (Orphanet:93262)
Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome (Orphanet:2229)
Distal monosomy 10p (Orphanet:1580)
Distal monosomy 10q (Orphanet:96148)
Dysmorphism - pectus carinatum - joint laxity (Orphanet:2104)
Dysostosis, Stanescu type (Orphanet:1798)
Encephalopathy due to beta-mercaptolactate-cysteine disulfiduria (Orphanet:1035)
FACIAL DYSMORPHISM, LENS DISLOCATION, ANTERIOR SEGMENT ABNORMALITIES,AND SPONTANEOUS FILTERING BLEBS (OMIM:601552)
Familial cutaneous telangiectasia and oropharyngeal predisposition cancer syndrome (Orphanet:313846)
Generalized resistance to thyroid hormone (Orphanet:3221)
Hallermann-Streiff syndrome (Orphanet:2108)
Hutchinson-Gilford progeria syndrome (Orphanet:740)
Hypospadias - intellectual deficit, Goldblatt type (Orphanet:2261)
Infantile spasms - broad thumbs (Orphanet:3173)
Isolated cloverleaf skull syndrome (Orphanet:2343)
Jackson-Weiss syndrome (Orphanet:1540)
Johanson-Blizzard syndrome (Orphanet:2315)
LAMBOTTE SYNDROME (OMIM:245552)
Lipodystrophy due to peptidic growth factors deficiency (Orphanet:1979)
Lowry-MacLean syndrome (Orphanet:2409)
MOVED TO 210600 (OMIM:608664)
Mandibular hypoplasia-deafness-progeroid syndrome (Orphanet:363649)
Mandibuloacral dysplasia (Orphanet:2457)
Mandibuloacral dysplasia with type B lipodystrophy (Orphanet:90154)
Mesomelia-synostoses syndrome (Orphanet:2496)
Metaphyseal chondrodysplasia, Kaitila type (Orphanet:166038)
Metaphyseal dysplasia - maxillary hypoplasia - brachydacty (Orphanet:2504)
Microcephalic osteodysplastic dysplasia, Saul-Wilson type (Orphanet:85172)
Microcephalic osteodysplastic primordial dwarfism types 1 and 3 (Orphanet:2636)
Microcephaly - cervical spine fusion anomalies (Orphanet:2522)
Nestor-Guillermo progeria syndrome (Orphanet:280576)
Nijmegen breakage syndrome (Orphanet:647)
Non-distal trisomy 10q (Orphanet:1695)
OSTEOGENESIS IMPERFECTA, TYPE II (OMIM:166210)
Occipital horn syndrome (Orphanet:198)
Osteogenesis imperfecta (Orphanet:666)
Osteogenesis imperfecta type 2 (Orphanet:216804)
Permanent neonatal diabetes mellitus - pancreatic and cerebellar agenesis (Orphanet:65288)
Prolidase deficiency (Orphanet:742)
Pseudoprogeria syndrome (Orphanet:2985)
Radio-renal syndrome (Orphanet:3015)
Renal-genital-middle ear anomalies (Orphanet:1092)
Rubinstein-Taybi syndrome (Orphanet:783)
Rubinstein-Taybi syndrome due to 16p13.3 microdeletion (Orphanet:353281)
Rubinstein-Taybi syndrome due to CREBBP mutations (Orphanet:353277)
Rubinstein-Taybi syndrome due to EP300 haploinsufficiency (Orphanet:353284)
Ruvalcaba syndrome (Orphanet:3121)
SECKEL SYNDROME 1 (OMIM:210600)
SECKEL SYNDROME 8 (OMIM:615807)
Saethre-Chotzen syndrome (Orphanet:794)
Sanjad-Sakati syndrome (Orphanet:2323)
Say-Barber-Miller syndrome (Orphanet:3132)
Seckel syndrome (Orphanet:808)
Temtamy syndrome (Orphanet:1777)
Tetraploidy (Orphanet:3305)
Trigonocephaly - broad thumbs (Orphanet:3365)
Trigonocephaly - short stature - developmental delay (Orphanet:3369)
Ulbright-Hodes syndrome (Orphanet:3404)
VITILIGO, PROGRESSIVE, WITH MENTAL RETARDATION AND URETHRAL DUPLICATION (OMIM:277465)
Van den Ende-Gupta syndrome (Orphanet:2460)
Werner syndrome (Orphanet:902)
Wiedemann-Rautenstrauch syndrome (Orphanet:3455)
Wolf-Hirschhorn syndrome (Orphanet:280)