Underdeveloped nasal alae
Symptom Information:
Symptom ID: | HPO:0000430 | ||||||||||||||||||||||||||
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) 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: |
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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) |