Prominent nose
Symptom Information:
Symptom ID: | HPO:0000448 | |||||||
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) Prominent nose(HPO:0000448) MedDRA: |
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Database Frequency: | 56 / 7739 | |||||||
Resource: |
All diseases associated with this symptom:
AREDYLD syndrome | (Orphanet:1133) |
Acrofacial dysostosis, Rodriguez type | (Orphanet:1788) |
Alopecia - contractures - dwarfism - intellectual deficit | (Orphanet:1005) |
Autosomal dominant nonsyndromic intellectual deficit | (Orphanet:178469) |
Autosomal recessive deafness-onychodystrophy syndrome | (Orphanet:79500) |
Beckwith-Wiedemann syndrome due to 11p15 microdeletion | (Orphanet:231127) |
Blepharophimosis-intellectual deficit syndrome, MKB type | (Orphanet:293707) |
Bloom syndrome | (Orphanet:125) |
Bowen-Conradi syndrome | (Orphanet:1270) |
CHROMOSOME 5q12 DELETION SYNDROME | (OMIM:615668) |
CUTIS VERTICIS GYRATA, RETINITIS PIGMENTOSA, AND SENSORINEURAL DEAFNESS | (OMIM:605685) |
Cooks syndrome | (Orphanet:1487) |
DERMATOLEUKODYSTROPHY | (OMIM:221790) |
DEXTROCARDIA WITH UNUSUAL FACIES AND MICROPHTHALMIA | (OMIM:221950) |
Distal monosomy 10q | (Orphanet:96148) |
FACIAL DYSMORPHISM, LENS DISLOCATION, ANTERIOR SEGMENT ABNORMALITIES,AND SPONTANEOUS FILTERING BLEBS | (OMIM:601552) |
Floating-Harbor syndrome | (Orphanet:2044) |
Galloway-Mowat syndrome | (Orphanet:2065) |
Genitopatellar syndrome | (Orphanet:85201) |
Hall-Riggs syndrome | (Orphanet:2107) |
Intellectual deficit, Buenos-Aires type | (Orphanet:3079) |
Intellectual deficit, X-linked - Dandy-Walker malformation - basal ganglia disease - Seizures | (Orphanet:1568) |
Intellectual deficit, X-linked - dysmorphism - cerebral atrophy | (Orphanet:2958) |
Jawad syndrome | (Orphanet:313795) |
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 15 | (OMIM:614202) |
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 39 | (OMIM:615541) |
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 5 | (OMIM:611091) |
MICROCEPHALY 13, PRIMARY, AUTOSOMAL RECESSIVE | (OMIM:616051) |
MICROCEPHALY AND CHORIORETINOPATHY, AUTOSOMAL RECESSIVE, 2 | (OMIM:616171) |
McDonough syndrome | (Orphanet:2471) |
Microcephalic osteodysplastic primordial dwarfism type 2 | (Orphanet:2637) |
Microcephalic osteodysplastic primordial dwarfism types 1 and 3 | (Orphanet:2636) |
Microcephalic primordial dwarfism, Dauber type | (Orphanet:319675) |
Microcephaly-cerebellar hypoplasia-cardiac conduction defect syndrome | (Orphanet:329332) |
Monosomy 18q | (Orphanet:1600) |
Mucopolysaccharidosis type 2, attenuated form | (Orphanet:217093) |
Nakajo-Nishimura syndrome | (Orphanet:2615) |
Nance-Horan syndrome | (Orphanet:627) |
Neonatal hemochromatosis | (Orphanet:446) |
OPITZ-KAVEGGIA SYNDROME | (OMIM:305450) |
PROGEROID FACIAL APPEARANCE WITH HAND ANOMALIES | (OMIM:602249) |
Primordial short stature - microdontia - opalescent and rootless teeth | (Orphanet:46658) |
Pseudoleprechaunism syndrome, Patterson type | (Orphanet:2976) |
Pycnodysostosis | (Orphanet:763) |
Radio-ulnar synostosis - intellectual deficit - hypotonia | (Orphanet:3270) |
Richieri Costa-Pereira syndrome | (Orphanet:3102) |
Rubinstein-Taybi syndrome due to 16p13.3 microdeletion | (Orphanet:353281) |
Rubinstein-Taybi syndrome due to EP300 haploinsufficiency | (Orphanet:353284) |
SECKEL SYNDROME 1 | (OMIM:210600) |
SECKEL SYNDROME 2 | (OMIM:606744) |
SPASTIC PARAPLEGIA 52, AUTOSOMAL RECESSIVE | (OMIM:614067) |
Schilbach-Rott syndrome | (Orphanet:2353) |
Seckel syndrome | (Orphanet:808) |
Short stature-onychodysplasia-facial dysmorphism-hypotrichosis syndrome | (Orphanet:314394) |
Short-rib thoracic dysplasia 13 with or without polydactyly | (OMIM:616300) |
Stormorken-Sjaastad-Langslet syndrome | (Orphanet:3204) |