Hearing Loss Disease Portal


 
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Most Common: Hearing Loss (D034381), Deafness (D003638), Sensorineural HL (D006319), Waardenburg Syndrome, Usher Syndromes
Disease Browser
Parent Node:
expandFoot Deformities, Congenital (D005532)
Parent Node:
expandHand Deformities, Congenital (D006228)
Parent Node:
expandPolydactyly (D017689)
Parent Node:
expandTooth Abnormalities (D014071)
..Starting node
..expandPolydactyly, Postaxial, with Dental and Vertebral Anomalies (C564880)

       Child Nodes:



 Sister Nodes: 
..expandAckerman syndrome (C538170)
..expandAnodontia (D000848) Child29
..expandAREDYLD Syndrome (C537427)
..expandBlepharo-cheilo-dontic syndrome (C536188)
..expandBook Syndrome (C562993)
..expandCarabelli Anomaly of Maxillary Molar Teeth (C566175)
..expandCleidocranial Dysplasia, Forme Fruste, Dental Anomalies Only (C563974)
..expandCODAS syndrome (C536434)
..expandDeafness with Labyrinthine Aplasia Microtia and Microdontia (LAMM) (C548011)
..expandDeafness, Congenital, and Onychodystrophy, Autosomal Dominant (C567274)
..expandDeafness, Congenital, with Inner Ear Agenesis, Microtia, and Microdontia (C565195)
..expandDens in Dente (D003719) Child1
..expandDental Enamel Hypoplasia (D003744) Child29
..expandDentin Dysplasia (D003805) Child3
..expandDentinogenesis Imperfecta (D003811) Child7
..expandDermoodontodysplasia (C565103)
..expandDiastema, Dental Medial (C565098)
..expandEuhidrotic ectodermal dysplasia (C535763)
..expandFacial Dysmorphism, Selective Tooth Agenesis, and Choroid Calcification (C567039)
..expandFaciocardiomelic Dysplasia, Lethal (C565578)
..expandFused Teeth (D005671)
..expandGrubben de Cock Borghgraef syndrome (C537621)
..expandHypoglossia-Hypodactylia (C566308)
..expandIridogoniodysgenesis, dominant type (C535536)
..expandKallmann Syndrome 2 with Selective Tooth Agenesis (C566948)
..expandKBG syndrome (C537015)
..expandLacrimoauriculodentodigital syndrome (C538132)
..expandLarsen syndrome, dominant type (C537873)
..expandNance-Horan syndrome (C538336)
..expandOculodentodigital Dysplasia (C563160)
..expandOculodentodigital Dysplasia, Autosomal Recessive (C567605)
..expandOculotrichodysplasia (C564934)
..expandOdontodysplasia (D018126) Child3
..expandOdontomicronychial dysplasia (C537741)
..expandOdontotrichoungual-Digital-Palmar Syndrome (C566598)
..expandOroacral Syndrome, Verloes-Koulischer Type (C566374)
..expandOtodental Dysplasia (C563482)
..expandPolydactyly, Postaxial, with Dental and Vertebral Anomalies (C564880)
..expandRodrigues blindness (C535865)
..expandSpondyloepimetaphyseal Dysplasia With Abnormal Dentition (C566644)
..expandTaurodontism (C536946)
..expandTaurodontism, microdontia, and dens invaginatus (C536947)
..expandTeeth noneruption of with maxillary hypoplasia and genu valgum (C536952)
..expandTeeth, Odd Shapes Of (C566076)
..expandTemtamy preaxial brachydactyly syndrome (C536958)
..expandTooth Agenesis, Selective, 2 (C566513)
..expandTooth Agenesis, Selective, 3 (C567036)
..expandTooth Agenesis, Selective, 4 (C563634)
..expandTooth Agenesis, Selective, 5 (C565757)
..expandTooth Agenesis, Selective, 6 (C567755)
..expandTooth Agenesis, Selective, X-Linked, 1 (C567060)
..expandTooth, Supernumerary (D014096) Child3
..expandTricho-dento-osseous syndrome 1 (C536550)
..expandTRICHODENTOOSSEOUS SYNDROME (OMIM:190320)
..expandWeyers acrofacial dysostosis (C536695)
..expandZazam Sheriff Phillips syndrome (C536723)
   

Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
Term ID:9077
Name:Polydactyly, Postaxial, with Dental and Vertebral Anomalies
Definition:
Alternative IDs:
ParentIDs:MESH:D005532|MESH:D006228|MESH:D014071|MESH:D017689
TreeNumbers:C05.330.495/C564880 |C05.390.408/C564880 |C05.660.585.512.380/C564880 |C05.660.585.600/C564880 |C05.660.585.988.425/C564880 |C07.650.800/C564880 |C07.793.700/C564880 |C16.131.621.585.380/C564880 |C16.131.621.585.425/C564880 |C16.131.621.585.600/C564880 |C16.131.85
Synonyms:
Slim Mappings:Congenital abnormality|Mouth disease|Musculoskeletal disease
Reference: MedGen: C564880
MeSH: C564880
OMIM: 263540;

Genes:
Phenotypes
1 HP:0000007Autosomal recessive inheritance
2 HP:00046912-3 toe syndactyly
3 HP:0000193Bifid uvula
4 HP:0001156Brachydactyly
5 HP:0001837Broad toe
6 HP:0004209Clinodactyly of the 5th finger
7 HP:0011088Dens in dente
8 HP:0006297Enamel hypoplasia
9 HP:0000286Epicanthus
10 HP:0002937Hemivertebrae
11 HP:0000668Hypodontia
12 HP:0008479Hypoplastic vertebral bodies
13 HP:0002751Kyphoscoliosis
14 HP:0002162Low posterior hairline
15 HP:0000369Low-set ears
16 HP:0001572Macrodontia
17 HP:0000303Mandibular prognathia
18 HP:0000774Narrow chest
19 HP:0000768Pectus carinatum
20 HP:0000767Pectus excavatum
21 HP:0001830Postaxial foot polydactyly
22 HP:0001162Postaxial hand polydactyly
23 HP:0005819Short middle phalanx of finger
24 HP:0006045Short pointed phalanges
25 HP:0003416Spinal canal stenosis
26 HP:0008368Tarsal synostosis
27 HP:0001770Toe syndactyly
28 HP:0008577Underfolded helix
29 HP:0002948Vertebral fusion
30 HP:0000465Webbed neck
Disease Causing ClinVar Variants