| Disease Browser
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Parent Node:
 Brachydactyly (D059327) |
..Starting node
.. Brachydactyly type A6 (C537092)
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Child Nodes:
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Sister Nodes: |
..Acrocapitofemoral Dysplasia (C564334)
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..Anonychia-onychodystrophy with brachydactyly type B and ectrodactyly (C536379)
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..Arterial Occlusive Disease, Progressive, with Hypertension, Heart Defects, Bone Fragility, and Brachysyndactyly (C566529)
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..Berk-Tabatznik syndrome (C535432)
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..Bork Stender Schmidt syndrome (C536576)
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..Brachydactyly preaxial with hallux varus and thumb abduction (C537087)
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..Brachydactyly type A1 (C537088)
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..Brachydactyly type A2 (C537089)
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..Brachydactyly type A3 (C537090)
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..Brachydactyly type A5 nail dysplasia (C537091)
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..Brachydactyly type A6 (C537092)
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..Brachydactyly type C (C537093)
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..Brachydactyly types B and E combined (C537094)
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..Brachydactyly with hypertension (C537095)
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..Brachydactyly, Coloboma, And Anterior Segment Dysgenesis (C566484)
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..Brachydactyly, Intraventricular Septal Defect, And Deafness (C566521)
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..Brachydactyly, Long-Thumb Type (C566204)
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..Brachydactyly, Type A1, B (C564635)
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..Brachydactyly, Type A2, With Microcephaly (C565894)
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..Brachydactyly, Type B1 (C566196)
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..BRACHYDACTYLY, TYPE B2 (OMIM:611377)
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..Brachydactyly, Type D (C562420)
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..Brachydactyly, Type E (C566194)  1
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..Brachydactyly, Type E, with Atrial Septal Defect, Type II (C566193)
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..BRACHYDACTYLY-MENTAL RETARDATION SYNDROME (OMIM:600430)
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..Brachydactyly-Nystagmus-Cerebellar Ataxia (C566192)
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..Brachydactyly-Syndactyly Syndrome (C565193)
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..Brachymesophalangy 2 and 5 (C537097)
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..Cleidocranial Dysplasia, Forme Fruste, With Brachydactyly (C566119)
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..Coloboma of Macula and Skeletal Anomalies (C565686)
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..Coloboma of macula type B brachydactyly (C535969)
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..Cryptomicrotia brachydactyly syndrome (C536219)
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..Digital Arthropathy-Brachydactyly, Familial (C564656)
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..Exostoses with Anetodermia and Brachydactyly, Type E (C565034)
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..Fibular aplasia ectrodactyly (C537930)
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..Fibular hypoplasia and complex brachydactyly (C537931)
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..Fitzsimmons-Guilbert syndrome (C537938)
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..GOMBO syndrome (C537284)
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..Heart-hand syndrome, Spanish type (C535853)
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..Hirschsprung disease type d brachydactyly (C538319)
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..Metaphyseal Dysplasia with Maxillary Hypoplasia and Brachydactyly (C563586)
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..MULTIPLE SYNOSTOSES SYNDROME 1 (OMIM:186500)
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..Prata Libéral Gonçalves syndrome (C538277)
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..Prolonged Bleeding Time, Brachydactyly, and Mental Retardation (C564207)
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..Robin Sequence with Distinctive Facial Appearance and Brachydactyly (C563880)
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..Short Stature, Facial Dysmorphism, Severe Brachydactyly, and Syndactyly (C567093)
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..Sillence syndrome (C537338)
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..Spondyloepiphyseal Dysplasia-Brachydactyly and Distinctive Speech (C567128)
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..Synostosis, Carpal, with Dysplastic Elbow Joints and Brachydactyly (C566090)
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..Temtamy preaxial brachydactyly syndrome (C536958)
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..Thumbs, Stiff, With Brachydactyly Type A1 And Developmental Delay (C566053)
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..Tonoki syndrome (C536967)
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..Ulnar/Fibular Ray Defect and Brachydactyly (C563905)
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Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
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