Prominent nose

Symptom Information:

Symptom ID: HPO:0000448
Synonyms:
Disproportionately large nose [HPO:0000448]
Large nose [HPO:0000448]
Prominent Nose [Orphanet:8060]
Disproportionately large nose [OMIM:Disproportionately large nose]
Large nose [OMIM:Large nose]
Prominent nose [OMIM:Prominent nose]
Long/large/bulbous nose [Orphanet:8060]
Quality:
Cross references:
Orphanet:8060 "Long/large/bulbous nose" [Orphanet:8060]
OMIM: "Disproportionately large nose" [OMIM:Disproportionately large nose]
OMIM: "Large nose" [OMIM:Large nose]
OMIM: "Prominent nose" [OMIM:Prominent nose]
Is a (Direct Parents):
HPO         Abnormal nasal morphology
Orphanet Abnormality of the nose
Orphanet Bulbous 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)
                      Prominent nose(HPO:0000448)
MedDRA:
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)