Depressed nasal ridge
Symptom Information:
Symptom ID: | HPO:0000457 | |||||
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) Abnormal nasal morphology(HPO:0005105) Depressed nasal ridge(HPO:0000457) MedDRA: |
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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) |