Underdeveloped nasal alae

Symptom Information:

Symptom ID: HPO:0000430
Synonyms:
Ala nasi, underdeveloped [HPO:0000430]
Alar cartilage hypoplasia [HPO:0000430]
Hypoplastic alae nasae [HPO:0000430]
Hypoplastic alae nasi [HPO:0000430]
Hypoplastic alar cartilage [HPO:0000430]
Hypoplastic alar nasae [HPO:0000430]
Hypoplastic nares [HPO:0000430]
Hypoplastic nasal alae [HPO:0000430]
Hypoplastic nasal wings [HPO:0000430]
Hypoplastic nostrils [HPO:0000430]
Nasal cartilage hypoplasia [HPO:0000430]
Thin hypoplastic alae nasi [HPO:0000430]
Underdeveloped Ala Nasi [Orphanet:8480]
Alar cartilage hypoplasia [OMIM:Alar cartilage hypoplasia]
Hypoplastic alae nasae [OMIM:Hypoplastic alae nasae]
Hypoplastic alae nasi [OMIM:Hypoplastic alae nasi]
Hypoplastic alar cartilage [OMIM:Hypoplastic alar cartilage]
Hypoplastic alar nasae [OMIM:Hypoplastic alar nasae]
Hypoplastic nares [OMIM:Hypoplastic nares]
Hypoplastic nasal alae [OMIM:Hypoplastic nasal alae]
Hypoplastic nasal wings [OMIM:Hypoplastic nasal wings]
Hypoplastic nostrils [OMIM:Hypoplastic nostrils]
Nasal cartilage hypoplasia [OMIM:Nasal cartilage hypoplasia]
Thin hypoplastic alae nasi [OMIM:Thin hypoplastic alae nasi]
Thin/hypoplastic ala nasi [Orphanet:8480]
Hypoplastic nasal alae (slight) [OMIM:Hypoplastic nasal alae (slight)]
Quality:
Cross references:
Orphanet:8480 "Thin/hypoplastic ala nasi" [Orphanet:8480]
OMIM: "Alar cartilage hypoplasia" [OMIM:Alar cartilage hypoplasia]
OMIM: "Hypoplastic alae nasae" [OMIM:Hypoplastic alae nasae]
OMIM: "Hypoplastic alae nasi" [OMIM:Hypoplastic alae nasi]
OMIM: "Hypoplastic alar cartilage" [OMIM:Hypoplastic alar cartilage]
OMIM: "Hypoplastic alar nasae" [OMIM:Hypoplastic alar nasae]
OMIM: "Hypoplastic nares" [OMIM:Hypoplastic nares]
OMIM: "Hypoplastic nasal alae" [OMIM:Hypoplastic nasal alae]
OMIM: "Hypoplastic nasal wings" [OMIM:Hypoplastic nasal wings]
OMIM: "Hypoplastic nostrils" [OMIM:Hypoplastic nostrils]
OMIM: "Nasal cartilage hypoplasia" [OMIM:Nasal cartilage hypoplasia]
OMIM: "Thin hypoplastic alae nasi" [OMIM:Thin hypoplastic alae nasi]
OMIM: "Hypoplastic nasal alae (slight)" [OMIM:Hypoplastic nasal alae (slight)]
Is a (Direct Parents):
HPO         Aplasia/Hypoplasia involving the nose
Orphanet Abnormality of the nose
HPO         Abnormality of the nasal alae
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)
                   Abnormality of the external nose(HPO:0010938)
                      Abnormality of the nasal alae(HPO:0000429)
                         Underdeveloped nasal alae(HPO:0000430)
                   Abnormal nasal morphology(HPO:0005105)
                      Aplasia/Hypoplasia involving the nose(HPO:0009924)
                         Underdeveloped nasal alae(HPO:0000430)
MedDRA:
Database Frequency: 90 / 7739
Resource:

All diseases associated with this symptom:

14q22q23 microdeletion syndrome (Orphanet:264200)
15q24 microdeletion syndrome (Orphanet:94065)
19q13.11 microdeletion syndrome (Orphanet:217346)
2q37 microdeletion syndrome (Orphanet:1001)
8q21.11 microdeletion syndrome (Orphanet:284160)
ARTHROGRYPOSIS, DISTAL, TYPE 2A (OMIM:193700)
Ablepharon macrostomia syndrome (Orphanet:920)
Acro-oto-ocular syndrome (Orphanet:2980)
Alar cartilages hypoplasia - coloboma - telecanthus (Orphanet:2007)
Auriculoocular anomalies - cleft lip (Orphanet:71270)
Baller-Gerold syndrome (Orphanet:1225)
Barber-Say syndrome (Orphanet:1231)
Bartsocas-Papas syndrome (Orphanet:1234)
Bazex-Dupré-Christol syndrome (Orphanet:113)
Blepharonasofacial malformation syndrome (Orphanet:1252)
Boomerang dysplasia (Orphanet:1263)
Choanal atresia - deafness - cardiac defects - dysmorphism (Orphanet:1200)
Cooks syndrome (Orphanet:1487)
Craniofacial dyssynostosis (Orphanet:1516)
Deafness-craniofacial syndrome (Orphanet:3241)
Distal 22q11.2 microdeletion syndrome (Orphanet:261330)
Distal monosomy 6p (Orphanet:96125)
Epidermolysis bullosa simplex with pyloric atresia (Orphanet:158684)
FRONTOFACIONASAL DYSPLASIA (OMIM:229400)
Faciocardiorenal syndrome (Orphanet:1973)
Femoral-facial syndrome (Orphanet:1988)
Fetal Gaucher disease (Orphanet:85212)
Filippi syndrome (Orphanet:3255)
Flat face - microstomia - ear anomaly (Orphanet:1968)
Floating-Harbor syndrome (Orphanet:2044)
Fraser syndrome (Orphanet:2052)
Freeman-Sheldon syndrome (Orphanet:2053)
Fronto-facio-nasal dysostosis (Orphanet:1791)
Frontonasal dysplasia-severe microphthalmia-severe facial clefting syndrome (Orphanet:306542)
GRANDDAD SYNDROME (OMIM:138920)
Gingival fibromatosis - facial dysmorphism (Orphanet:2025)
Hallermann-Streiff syndrome (Orphanet:2108)
Hennekam-Beemer syndrome (Orphanet:2135)
Hepatic fibrosis - renal cysts - intellectual deficit (Orphanet:2031)
Hypoplastic tibiae - postaxial polydactyly (Orphanet:3332)
Johanson-Blizzard syndrome (Orphanet:2315)
KBG syndrome (Orphanet:2332)
KEPPEN-LUBINSKY SYNDROME (OMIM:614098)
Keutel syndrome (Orphanet:85202)
Koolen-De Vries syndrome (Orphanet:96169)
Laurin-Sandrow syndrome (Orphanet:2378)
MEIER-GORLIN SYNDROME 2 (OMIM:613800)
MENTAL RETARDATION, AUTOSOMAL DOMINANT 27 (OMIM:615866)
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 5 (OMIM:611091)
MULTIPLE SYNOSTOSES SYNDROME 1 (OMIM:186500)
Marden-Walker syndrome (Orphanet:2461)
McDonough syndrome (Orphanet:2471)
Microcephalic osteodysplastic primordial dwarfism type 2 (Orphanet:2637)
Microcephaly - cardiac defect - lung malsegmentation (Orphanet:2516)
Microcephaly - intellectual deficit - phalangeal and neurological anomalies (Orphanet:137658)
Multiple synostoses syndrome (Orphanet:3237)
Neurologic Waardenburg-Shah syndrome (Orphanet:163746)
OCULODENTODIGITAL DYSPLASIA (OMIM:164200)
OCULODENTODIGITAL DYSPLASIA, AUTOSOMAL RECESSIVE (OMIM:257850)
OTOFACIOOSSEOUS-GONADAL SYNDROME (OMIM:601976)
Oculodentodigital dysplasia (Orphanet:2710)
Oculomaxillofacial dysostosis (Orphanet:1794)
Orofaciodigital syndrome type 1 (Orphanet:2750)
PONTOCEREBELLAR HYPOPLASIA, TYPE 10 (OMIM:615803)
Potocki-Shaffer syndrome (Orphanet:52022)
Premature ageing appearance-developmental delay-cardiac arrhythmia syndrome (Orphanet:276432)
Prominent glabella - microcephaly - hypogenitalism (Orphanet:2083)
RAPP-HODGKIN SYNDROME (OMIM:129400)
ROBERTS SYNDROME (OMIM:268300)
Roberts syndrome (Orphanet:3103)
Ruvalcaba syndrome (Orphanet:3121)
SC PHOCOMELIA SYNDROME (OMIM:269000)
SECKEL SYNDROME 4 (OMIM:613676)
SHORT syndrome (Orphanet:3163)
SIMOSA CRANIOFACIAL SYNDROME (OMIM:182150)
STEVENSON-CAREY SYNDROME (OMIM:611961)
SYNOSTOSES, TARSAL, CARPAL, AND DIGITAL (OMIM:186400)
Stapes ankylosis with broad thumbs and toes (Orphanet:140917)
TRICHORHINOPHALANGEAL SYNDROME, TYPE III (OMIM:190351)
Tarsal-carpal coalition syndrome (Orphanet:1412)
VELOCARDIOFACIAL SYNDROME (OMIM:192430)
Van den Ende-Gupta syndrome (Orphanet:2460)
WAARDENBURG SYNDROME, TYPE 2A (OMIM:193510)
WHISTLING FACE SYNDROME, RECESSIVE FORM (OMIM:277720)
Waardenburg syndrome (Orphanet:3440)
Waardenburg syndrome type 1 (Orphanet:894)
Waardenburg syndrome type 2 (Orphanet:895)
Waardenburg-Shah syndrome (Orphanet:897)
X-linked hypohidrotic ectodermal dysplasia (Orphanet:181)
Zechi-Ceide syndrome (Orphanet:217017)