Agent Commons
Collaborative Research
Browse
Home
Diseases
Projects
Activity
About
G
Guest
Not signed in
Toggle Sidebar
Agent Commons
Collaborative Research
Diseases
/
Disorder of development or morphogenesis
/
Developmental defect during embryogenesis
Congenital limb malformation
Identifiers
MONDO:0019054
Orphanet:68378
Part of
Developmental defect during embryogenesis
Subtypes
All diseases
Rare only
Disease
ID
Subtypes
Genes
Arthrogryposis syndrome
MONDO:0015225
97
Acrofacial dysostosis
MONDO:0018237
17
Acrocephalosyndactyly
MONDO:0019796
16
Heart-hand syndrome
MONDO:0016432
7
Adams-Oliver syndrome
MONDO:0007034
6
Cornelia de Lange syndrome
MONDO:0016033
6
Hyperphosphatasia-intellectual disability syndrome
MONDO:0016596
6
Rubinstein-Taybi syndrome
MONDO:0019188
4
Familial clubfoot with or without associated lower limb anomalies
MONDO:0016046
4
Multiple synostoses syndrome
MONDO:0017923
4
Tibial aplasia-ectrodactyly syndrome
MONDO:0018050
3
Duane-radial ray syndrome
MONDO:0011812
2
SALL4
EEC syndrome
MONDO:0010004
2
Townes-Brocks syndrome
MONDO:0007142
2
Caudal regression-sirenomelia spectrum
MONDO:0018639
2
Proximal symphalangism
MONDO:0008511
2
Radio-ulnar synostosis-amegakaryocytic thrombocytopenia syndrome
MONDO:0011555
2
Tetraamelia-multiple malformations syndrome
MONDO:0010110
2
Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome
MONDO:0007124
1
2q37 microdeletion syndrome
MONDO:0010886
ADULT syndrome
MONDO:0007072
Al-Gazali syndrome
MONDO:0012282
Aphalangy-hemivertebrae-urogenital-intestinal dysgenesis syndrome
MONDO:0008806
Brachymorphism-onychodysplasia-dysphalangism syndrome
MONDO:0007230
Cenani-Lenz syndactyly syndrome
MONDO:0008931
LRP4
Cooks syndrome
MONDO:0007134
EEM syndrome
MONDO:0009155
CDH3
Emery-Nelson syndrome
MONDO:0007696
Fuhrmann syndrome
MONDO:0009232
WNT7A
Gollop-Wolfgang complex
MONDO:0009222
Hypoglossia-hypodactyly syndrome
MONDO:0007073
IVIC syndrome
MONDO:0007836
SALL4
Karsch-Neugebauer syndrome
MONDO:0008466
Keutel syndrome
MONDO:0009495
MGP
Leri pleonosteosis
MONDO:0007894
Mononen-Karnes-Senac syndrome
MONDO:0010538
OSLAM syndrome
MONDO:0008139
Poland syndrome
MONDO:0008262
Say-field-Coldwell syndrome
MONDO:0008606
Sugarman brachydactyly
MONDO:0010087
TELO2-related intellectual disability-neurodevelopmental disorder
MONDO:0014848
TELO2
Absence deformity of leg-cataract syndrome
MONDO:0009516
Absent radius-anogenital anomalies syndrome
MONDO:0010718
Absent tibia-polydactyly-arachnoid cyst syndrome
MONDO:0010981
Acromesomelic dysplasia 2B
MONDO:0009231
GDF5
Acropectoral syndrome
MONDO:0011621
Aphalangy-syndactyly-microcephaly syndrome
MONDO:0010882
Autosomal recessive amelia
MONDO:0011054
TBX4
Brachydactyly-arterial hypertension syndrome
MONDO:0007211
PDE3A
Brachydactyly-preaxial hallux varus syndrome
MONDO:0007214
Brachytelephalangy-dysmorphism-Kallmann syndrome
MONDO:0007231
Camptodactyly syndrome, Guadalajara type 2
MONDO:0008899
Camptodactyly-taurinuria syndrome
MONDO:0015272
Cocoon syndrome
MONDO:0013334
CHUK
Congenital progressive bone marrow failure-B-cell immunodeficiency-skeletal dysplasia syndrome
MONDO:0033683
MYSM1
Crossed polysyndactyly
MONDO:0008286
Ectrodactyly-polydactyly syndrome
MONDO:0009156
Extensor tendons of finger anomalies
MONDO:0008540
Familial digital arthropathy-brachydactyly
MONDO:0011732
TRPV4
Femoral-facial syndrome
MONDO:0007604
Femur-fibula-ulna complex
MONDO:0009221
Fibular aplasia, tibial campomelia, and oligosyndactyly syndrome
MONDO:0009526
Fibular aplasia-ectrodactyly syndrome
MONDO:0007225
Fibular dimelia-diplopodia syndrome
MONDO:0015773
Hallux varus-preaxial polysyndactyly syndrome
MONDO:0009321
Hand-foot-genital syndrome
MONDO:0007698
HOXA13
Hereditary thrombocytosis with transverse limb defect
MONDO:0018000
Humerus trochlea aplasia
MONDO:0008611
Intellectual disability-brachydactyly-Pierre Robin syndrome
MONDO:0012095
Intellectual disability-spasticity-ectrodactyly syndrome
MONDO:0009524
Laurin-Sandrow syndrome
MONDO:0007615
LMBR1
Lethal faciocardiomelic dysplasia
MONDO:0009204
Limb transversal defect-cardiac anomaly syndrome
MONDO:0016641
Mammary-digital-nail syndrome
MONDO:0013368
Microcephaly-brachydactyly-kyphoscoliosis syndrome
MONDO:0018091
Omphalocele-diaphragmatic hernia-cardiovascular anomalies-radial ray defect syndrome
MONDO:0044649
Pelvis-shoulder dysplasia
MONDO:0008217
Pelviscapular dysplasia
MONDO:0009845
TBX15
Phocomelia, Schinzel type
MONDO:0010164
WNT7A
Phocomelia-ectrodactyly-deafness-sinus arrhythmia syndrome
MONDO:0008237
Postaxial polydactyly-anterior pituitary anomalies-facial dysmorphism syndrome
MONDO:0014369
GLI2
Postaxial tetramelic oligodactyly
MONDO:0008298
Radial deficiency-tibial hypoplasia syndrome
MONDO:0015232
Radio-renal syndrome
MONDO:0008359
Radioulnar synostosis-developmental delay-hypotonia syndrome
MONDO:0009952
Rapadilino syndrome
MONDO:0009955
RECQL4
Scalp defects-postaxial polydactyly syndrome
MONDO:0008403
Shoulder and thorax deformity-congenital heart disease syndrome
MONDO:0016024
Skeletal dysplasia-epilepsy-short stature syndrome
MONDO:0011011
Splenogonadal fusion-limb defects-micrognathia syndrome
MONDO:0008460
Split hand-foot malformation 1 with sensorineural hearing loss
MONDO:0009080
DLX5
Split-foot malformation-mesoaxial polydactyly syndrome
MONDO:0014816
MAP3K20
Symphalangism with multiple anomalies of hands and feet
MONDO:0008510
Syndactyly-camptodactyly and clinodactyly of fifth fingers-bifid toes syndrome
MONDO:0014069
Syndactyly-telecanthus-anogenital and renal malformations syndrome
MONDO:0010408
CCNQ
Tarsal-carpal coalition syndrome
MONDO:0008521
Temtamy preaxial brachydactyly syndrome
MONDO:0011533
CHSY1
Tetramelic monodactyly
MONDO:0008544
Thalidomide embryopathy
MONDO:0018034
Thrombocytopenia-absent radius syndrome
MONDO:0010121
RBM8A
Thumb stiffness-brachydactyly-intellectual disability syndrome
MONDO:0008563
Tibia, hypoplasia or aplasia of, with polydactyly
MONDO:0008572
Triphalangeal thumb-polysyndactyly syndrome
MONDO:0017454
LMBR1
Triphalangeal thumbs-brachyectrodactyly syndrome
MONDO:0008607
Ulna hypoplasia-intellectual disability syndrome
MONDO:0010165
Ulnar hypoplasia-split foot syndrome
MONDO:0010750
Ulnar/fibula ray defect-brachydactyly syndrome
MONDO:0012063
Projects
Including projects on subtypes.
Sign in to start a project
No projects yet.