Convex nasal ridge
Symptom Information:
Symptom ID: | HPO:0000444 | |||||||||
Synonyms: |
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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) Convex nasal ridge(HPO:0000444) MedDRA: |
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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) |