| Disease Browser
|
Parent Node:
 dysostosis of genetic origin with limb anomaly as a major feature (MONDO:0018455) |
..Starting node
.. syndactyly (disease) ()
|
Child Nodes:
|
| ........ectodermal dysplasia-syndactyly syndrome () |
| ........non-syndromic syndactyly () |
| ........synpolydactyly () |
Sister Nodes: |
..absence deformity of leg-cataract syndrome ()
|
..absent radius-anogenital anomalies syndrome ()
|
..absent tibia-polydactyly syndrome ()
|
..Adams-Oliver syndrome ()
|
..ADULT syndrome ()
|
..Aphalangy-hemivertebrae-urogenital-intestinal dysgenesis syndrome ()
|
..autosomal recessive amelia ()
|
..bipartite talus ()
|
..brachydactyly (disease) ()
|
..camptodactyly syndrome, Guadalajara type 2 ()
|
..camptodactyly syndrome, Guadalajara type 3 ()
|
..camptodactyly with fibrous tissue hyperplasia and skeletal dysplasia ()
|
..camptodactyly, myopia, and fibrosis of the medial rectus muscle of eye ()
|
..congenital pseudoarthrosis of the limbs ()
|
..Cornelia de Lange syndrome ()
|
..Duane-radial ray syndrome ()
|
..dysostosis with combined reduction defects of upper and lower limbs ()
|
..dysostosis with limb and face anomalies as a major feature ()
|
..EEC syndrome ()
|
..EEM syndrome ()
|
..external auditory canal atresia-vertical talus-hypertelorism syndrome ()
|
..familial clubfoot with or without associated lower limb anomalies ()
|
..Fanconi anemia ()
|
..femoral-facial syndrome ()
|
..fibular hypoplasia and complex brachydactyly ()
|
..heart-hand syndrome ()
|
..hereditary thrombocytosis with transverse limb defect ()
|
..humerus trochlea aplasia ()
|
..IVIC syndrome ()
|
..joint formation defects ()
|
..Karsch-Neugebauer syndrome ()
|
..lethal faciocardiomelic dysplasia ()
|
..limb transversal defect-cardiac anomaly syndrome ()
|
..limb-mammary syndrome ()
|
..mammary-digital-nail syndrome ()
|
..non-syndromic limb reduction defect ()
|
..non-syndromic polydactyly, syndactyly and/or hyperphalangy ()
|
..omphalocele-diaphragmatic hernia-cardiovascular anomalies-radial ray defect syndrome ()
|
..otoonychoperoneal syndrome ()
|
..pelvis-shoulder dysplasia ()
|
..pelviscapular dysplasia ()
|
..phocomelia, Schinzel type ()
|
..phocomelia-ectrodactyly-deafness-sinus arrhythmia syndrome ()
|
..polydactyly (disease) ()
|
..postaxial tetramelic oligodactyly ()
|
..radio-renal syndrome ()
|
..rapadilino syndrome ()
|
..Roberts syndrome ()
|
..shoulder and thorax deformity-congenital heart disease syndrome ()
|
..splenogonadal fusion-limb defects-micrognathia syndrome ()
|
..split hand-foot malformation 3 ()
|
..syndactyly (disease) ()
|
..syndrome with limb duplication, polydactyly, syndactyly, and/or hyperphalangy ()
|
..syndrome with synostosis or other joint formation defect ()
|
..tetraamelia-multiple malformations syndrome ()
|
..tetramelic monodactyly ()
|
..thrombocytopenia-absent radius syndrome ()
|
..ulna hypoplasia-intellectual disability syndrome ()
|
..ulnar-mammary syndrome ()
|
..X-linked keloid scarring-reduced joint mobility-increased optic cup-to-disc ratio syndrome ()
|
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM,ClinVar, CTD
|
: 
