Depressed nasal ridge

Symptom Information:

Symptom ID: HPO:0000457
Synonyms:
Depressed nasal ridge [Orphanet:8180]
Flat nose [OMIM:Flat nose]
Flattened nose [Orphanet:8180]
Flat nose. [OMIM:Flat nose.]
Flattened nose [OMIM:Flattened nose]
Quality:
Cross references:
Orphanet:8180 "Flattened nose" [Orphanet:8180]
OMIM: "Flat nose" [OMIM:Flat nose]
OMIM: "Flat nose." [OMIM:Flat nose.]
OMIM: "Flattened nose" [OMIM:Flattened nose]
Is a (Direct Parents):
HPO         Abnormal nasal morphology
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)
                   Abnormal nasal morphology(HPO:0005105)
                      Depressed nasal ridge(HPO:0000457)
MedDRA:
Database Frequency: 85 / 7739
Resource:

All diseases associated with this symptom:

1p36 deletion syndrome (Orphanet:1606)
22q11.2 microduplication syndrome (Orphanet:1727)
8q22.1 microdeletion syndrome (Orphanet:178303)
Acrodysostosis (Orphanet:950)
Alpha-mannosidosis (Orphanet:61)
Alpha-thalassemia - X-linked intellectual deficit syndrome (Orphanet:847)
Arthrogryposis multiplex congenita (Orphanet:1037)
Auriculoocular anomalies - cleft lip (Orphanet:71270)
Autosomal dominant hypohidrotic ectodermal dysplasia (Orphanet:1810)
Autosomal recessive polycystic kidney disease (Orphanet:731)
Bilateral renal agenesis (Orphanet:1848)
Blackfan-Diamond anemia (Orphanet:124)
Bone dysplasia, lethal Holmgren type (Orphanet:1842)
CEDNIK syndrome (Orphanet:66631)
Campomelic dysplasia (Orphanet:140)
Cartilage-hair hypoplasia (Orphanet:175)
Char syndrome (Orphanet:46627)
Chondrodysplasia punctata, tibial-metacarpal type (Orphanet:79346)
Cleft lip/palate - deafness - sacral lipoma (Orphanet:2003)
Coffin-Siris syndrome (Orphanet:1465)
Congenital hypothyroidism (Orphanet:442)
Craniofacial-deafness-hand syndrome (Orphanet:1529)
Craniofrontonasal dysplasia (Orphanet:1520)
Cutis laxa (Orphanet:209)
DIAMOND-BLACKFAN ANEMIA 1 (OMIM:105650)
Delayed membranous cranial ossification (Orphanet:3034)
Diaphanospondylodysostosis (Orphanet:66637)
Dislocation of the hip - dysmorphism (Orphanet:2412)
Distal 22q11.2 microduplication syndrome (Orphanet:261337)
Down syndrome (Orphanet:870)
Dysmorphism - pectus carinatum - joint laxity (Orphanet:2104)
Dysmorphism - short stature - deafness - disorder of sex development (Orphanet:2282)
Dyssegmental dysplasia, Silverman-Handmaker type (Orphanet:1865)
Ectodermal dysplasia, Berlin type (Orphanet:1816)
Epimetaphyseal skeletal dysplasia (Orphanet:1819)
Facial ectodermal dysplasia (Orphanet:1807)
Familial osteodysplasia, Anderson type (Orphanet:2769)
Fetal Gaucher disease (Orphanet:85212)
Fetal hydantoin syndrome (Orphanet:1912)
Fetal valproate syndrome (Orphanet:1906)
Fronto-facio-nasal dysostosis (Orphanet:1791)
Frontonasal dysplasia with alopecia and genital anomaly (Orphanet:228390)
GM1 gangliosidosis (Orphanet:354)
GM1 gangliosidosis type 1 (Orphanet:79255)
Harlequin ichthyosis (Orphanet:457)
Heart defect - round face - congenital developmental delay (Orphanet:1355)
Holoprosencephaly (Orphanet:2162)
Hyperlysinemia, type I (OMIM:238700)
Hypertelorism - hypospadias - polysyndactyly syndrome (Orphanet:2211)
Intellectual deficit - hypotonia - skin hyperpigmentation (Orphanet:3050)
Ito hypomelanosis (Orphanet:435)
Laron syndrome (Orphanet:633)
Lethal hemolytic anemia - genital anomalies (Orphanet:1046)
Lethal multiple pterygium syndrome (Orphanet:33108)
Lethal osteosclerotic bone dysplasia (Orphanet:1832)
MICROPHTHALMIA WITH CYST, BILATERAL FACIAL CLEFTS, AND LIMB ANOMALIES (OMIM:607597)
MIDLINE MALFORMATIONS, MULTIPLE, WITH LIMB ABNORMALITIES AND HYPOPITUITARISM (OMIM:601016)
Maxillo-nasal dysplasia (Orphanet:1248)
Meckel syndrome (Orphanet:564)
Meckel syndrome, type 8 (OMIM:613885)
Metaphyseal acroscyphodysplasia (Orphanet:1240)
Mosaic variegated aneuploidy syndrome (Orphanet:1052)
Mucopolysaccharidosis type 2 (Orphanet:580)
NEU-LAXOVA SYNDROME 2 (OMIM:616038)
Neu-Laxova syndrome (Orphanet:2671)
Non-rhizomelic chondrodysplasia punctata (Orphanet:176)
Noonan syndrome with multiple lentigines (Orphanet:500)
Orofaciodigital syndrome type 4 (Orphanet:2753)
Otopalatodigital syndrome (Orphanet:669)
Otospondylomegaepiphyseal dysplasia (Orphanet:1427)
PEROXISOME BIOGENESIS DISORDER 3B (OMIM:266510)
Prolidase deficiency (Orphanet:742)
Pyknoachondrogenesis (Orphanet:3003)
Rhizomelic dysplasia, Patterson-Lowry type (Orphanet:2831)
Short rib-polydactyly syndrome (Orphanet:1505)
Sotos syndrome (Orphanet:821)
Stickler syndrome (Orphanet:828)
Summitt syndrome (Orphanet:3210)
Syndromic diarrhea (Orphanet:84064)
Thoracic dysplasia-hydrocephalus syndrome (Orphanet:1861)
Ulna metaphyseal dysplasia syndrome (Orphanet:1837)
X-linked dominant chondrodysplasia, Chassaing-Lacombe type (Orphanet:163966)
X-linked hypohidrotic ectodermal dysplasia (Orphanet:181)
X-linked lethal multiple pterygium syndrome (Orphanet:79447)
Zunich-Kaye syndrome (Orphanet:3474)