Disease Browser
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Parent Node: Musculoskeletal Abnormalities (D009139) |
..Starting node ..Limb Deformities, Congenital (D017880)
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Child Nodes:
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........Aase Smith syndrome (C535332) |
........Abruzzo Erickson syndrome (C535559) |
........Acromegaloid facial appearance syndrome (C535655) |
........Acromicric dysplasia (C535662) 1 |
........Acropectoral syndrome (C535664) |
........Acropectorovertebral Dysplasia, F-Form (C566319) |
........Acrorenal syndrome recessive (C535666) |
........Adams Oliver syndrome (C538225) |
........Arachnodactyly (D054119) 10 |
........Arms, Malformation of (C566258) |
........ATELOSTEOGENESIS, TYPE III (OMIM:108721) |
........B-Cell Immunodeficiency, Distal Limb Anomalies, And Urogenital Malformations (C563745) |
........Bagatelle Cassidy syndrome (C537796) |
........Brachydactyly (D059327) 54 |
........Brachymorphism-onychodysplasia-dysphalangism syndrome (C536242) |
........Brachyolmia, recessive Hobaek type (C537099) |
........Calabro syndrome (C537960) |
........Camptobrachydactyly (C537967) |
........Cartwright Nelson Fryns syndrome (C535917) |
........Cerebrorenodigital Syndrome with Limb Malformations and Triradiate Acetabula (C563731) |
........Chondrodysplasia, acromesomelic, with genital anomalies (C537913) |
........COCOON SYNDROME (OMIM:613630) |
........Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects (C562515) |
........Corpus Callosum, Agenesis of, with Facial Anomalies and Robin Sequence (C563127) |
........Craniomicromelic Syndrome (C566522) |
........Diaphragmatic Defects, Limb Deficiencies, and Ossification Defects Of Skull (C563380) |
........Ectrodactyly (C574275) |
........Ectrodactyly-Polydactyly (C565601) |
........Ectromelia (D004480) 22 |
........Faciocardiomelic Dysplasia, Lethal (C565578) |
........Fetal akinesia syndrome, X-linked (C537921) |
........Foot Deformities, Congenital (D005532) 78 |
........Freire-Maia odontotrichomelic syndrome (C535637) |
........Fryns syndrome (C538070) |
........Genee-Wiedemann syndrome (C537680) |
........Grubben de Cock Borghgraef syndrome (C537621) |
........Hand and foot deformity with flat facies (C535626) |
........Hand Deformities, Congenital (D006228) 134 |
........Hanhart syndrome (C535629) |
........Heart defects limb shortening (C535850) |
........Hypochondroplasia (C562937) |
........Hypoglossia-Hypodactylia (C566308) |
........Ichthyosis tapered fingers midline groove up (C536272) |
........Kaplan Plauchu Fitch syndrome (C536892) |
........Kaufman oculocerebrofacial syndrome (C537013) |
........Krause-Kivlin syndrome (C537617) |
........Kuster syndrome (C538126) |
........Laryngeal Atresia, Encephalocele, and Limb Deformities (C564620) |
........Le Marec Bracq Picaud syndrome (C536997) |
........Limb Defects, Distal Transverse, with Mental Retardation and Spasticity (C565438) |
........Limb Deficiencies, Distal, with Micrognathia (C565437) |
........Limb-mammary syndrome (C535903) |
........Lower Extremity Deformities, Congenital (D038061) 89 |
........Lynch Lee Murday syndrome (C537713) |
........Megalodactyly (C562546) |
........Mental retardation spasticity ectrodactyly (C537446) |
........Mesomelia-synostoses syndrome (C537348) |
........Metaphyseal anadysplasia (C537351) |
........Metaphyseal Anadysplasia 1 (C567545) |
........Metaphyseal Anadysplasia 2 (C567771) |
........Microphthalmia with Cyst, Bilateral Facial Clefts, and Limb Anomalies (C564370) |
........Microphthalmia, Syndromic 6 (C566440) |
........Multiple Epiphyseal Dysplasia with Robin Phenotype (C563291) |
........Multiple Pterygium Syndrome, X-Linked (C564072) |
........Nephrosis deafness urinary tract digital malformation (C536402) |
........Neu Laxova syndrome (C536405) |
........Nievergelt syndrome (C536120) |
........Oculodigitoesophagoduodenal syndrome (C537734) |
........Palant cleft palate syndrome (C538102) |
........Penttinen-Aula syndrome (C536653) |
........Pointer syndrome (C536323) |
........Polydactyly (D017689) 61 |
........Postaxial Oligodactyly, Tetramelic (C566767) |
........Powell Chandra Saal syndrome (C538357) |
........Propping Zerres syndrome (C538052) |
........Proteus Syndrome (D016715) 1 |
........Radial Ray Deficiency, X-Linked (C564523) |
........Rapadilino syndrome (C535288) |
........Reardon Hall Slaney syndrome (C535294) |
........Renal dysplasia - limb defects syndrome (C537754) |
........Robinow Syndrome, Autosomal Dominant (C562492) |
........Robinow syndrome, autosomal recessive (C535863) |
........Ruzicka Goerz Anton syndrome (C537192) |
........Short Stature-Obesity Syndrome (C564821) |
........Splenogonadal fusion limb defects micrognatia (C537318) |
........Split hand foot deformity (C535777) 2 |
........Split hand foot deformity 1 (C567893) |
........Split-Hand And Split-Foot With Hypodontia (C566665) |
........Split-Hand Foot Malformation 2 (C564056) 1 |
........Split-Hand With Obstructive Uropathy, Spina Bifida, And Diaphragmatic Defects (C566662) |
........Split-Hand/Foot Malformation 4 (C565344) |
........Split-Hand/Foot Malformation 5 (C564674) |
........Split-Hand/Foot Malformation 6 (C567616) |
........Split-hand/foot malformation with long bone deficiency (C536425) |
........Split-Hand/Foot Malformation With Long Bone Deficiency 2 (C565199) |
........Split-Hand/Foot Malformation With Long Bone Deficiency 3 (C567245) |
........Steinfeld Syndrome (C566655) |
........Stern Lubinsky Durrie syndrome (C537488) |
........Stratton-Parker Syndrome (C566105) |
........Syndactyly (D013576) 69 |
........Terminal Osseous Dysplasia and Pigmentary Defects (C564554) |
........Tetramelic Monodactyly (C566066) |
........Thanatophoric Dysplasia (D013796) 8 |
........Thoracic Dysplasia-Hydrocephalus Syndrome (C564774) |
........Thoraco limb dysplasia Rivera type (C536516) |
........Thoracomelic Dysplasia (C564773) |
........Ulnar Hypoplasia with Mental Retardation (C564757) |
........Upper Extremity Deformities, Congenital (D038062) 145 |
........VACTERL association (C536495) |
........VACTERL association with hydrocephaly, X-linked (C536520) |
........VACTERL hydrocephaly (C536521) |
........Viljoen Kallis Voges syndrome (C536349) |
........Weyers acrofacial dysostosis (C536695) |
........Wright Dyck syndrome (C536749) |
........Yunis Varon syndrome (C536719) |
Sister Nodes: |
..Absent patella (C535568)
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..ACROPECTOROVERTEBRAL DYSPLASIA (OMIM:102510)
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..Arthrogryposis (D001176) 55
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..Campomelic Dysplasia (D055036) 6
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..Cervical Rib Syndrome (D002573) 1
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..Chondrodysplasia, Grebe type (C537915)
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..Congenital absence of gluteal muscles (C535561)
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..Congenital absence of the sternocleidomastoid muscle (C535977)
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..Congenital Lipomatous Overgrowth, Vascular Malformations, and Epidermal Nevi (C567863)
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..Craniofacial Abnormalities (D019465) 685
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..Funnel Chest (D005660) 4
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..Gastroschisis (D020139) 1
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..Hajdu-Cheney Syndrome (D031845) 1
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..Hip Dislocation, Congenital (D006618) 12
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..Klippel-Feil Syndrome (D007714) 5
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..Larsen syndrome, recessive type (C537874)
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..Laryngomalacia (D055092) 1
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..Limb Deformities, Congenital (D017880) 495
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..Pectus Carinatum (D066166)
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..Pseudoarthrogryposis (C566753)
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..Pterygium, Antecubital (C566738)
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..Sacrococcygeal dysgenesis association (C537225)
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..Sternal cleft (C537489)
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..Synostosis (D013580) 150
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..Tracheobronchomalacia (D055089) 4
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..VACTERL Association With Hydrocephalus (C564751)
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..Widow's Peak Syndrome (C564040)
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Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD
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