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Term:
SPLIT-FOOT MALFORMATION WITH MESOAXIAL POLYDACTYLY (DOID:9008338)
Annotations: Rat: (1) Mouse: (1) Human: (2) Chinchilla: (1) Bonobo: (1) Dog: (1) Squirrel: (1) Pig: (1)
Parent Terms Term With Siblings Child Terms
Aase Smith Syndrome 
Abruzzo Erickson Syndrome  
Acromegaloid Facial Appearance Syndrome 
Acromesomelic Dysplasia, Demirhan Type  
acromicric dysplasia +   
Acropectoral Syndrome 
Acropectorovertebral Dysplasia 
Adams-Oliver syndrome +   
ADULT syndrome  
Agenesis of Corpus Callosum with Facial Anomalies and Robin Sequence 
Arachnodactyly +   
asphyxiating thoracic dystrophy +   
Atelosteogenesis Type 3  
autosomal recessive Robinow syndrome  
B-Cell Immunodeficiency, Distal Limb Anomalies, and Urogenital Malformations 
Bagatelle Cassidy syndrome 
Biemond Syndrome II 
brachydactyly +   
Brachymorphism-Onychodysplasia-Dysphalangism Syndrome 
Brachyolmia Type 1, Hobaek Type 
Brachyphalangy, Polydactyly, and Tibial Aplasia/Hypoplasia 
Calabro Syndrome 
Camptobrachydactyly 
Cartwright Nelson Fryns Syndrome 
Cerebrorenodigital Syndrome with Limb Malformations and Triradiate Acetabula 
CHILD Syndrome  
CHITAYAT SYNDROME  
cocoon syndrome  
CONGENITAL CONTRACTURES OF THE LIMBS AND FACE, HYPOTONIA, AND DEVELOPMENTAL DELAY  
Craniomicromelic Syndrome 
Crossed Polydactyly, Type I  
Crossed Polysyndactyly 
Culler-Jones syndrome  
Desbuquois dysplasia +   
Diaphragmatic Defects, Limb Deficiencies, and Ossification Defects Of Skull 
Distal Transverse Limb Defects with Mental Retardation and Spasticity 
Ectrodactyly-Polydactyly 
Ectromelia +   
Faciocardiomelic Dysplasia, Lethal 
Feingold syndrome +   
Fetal Akinesia Syndrome, X-Linked 
Freire-Maia Odontotrichomelic Syndrome 
Fryns Syndrome 
Garret Tripp Syndrome 
Grubben de Cock Borghgraef Syndrome 
Hand and Foot Deformity with Flat Facies 
Hanhart Syndrome 
Heart Defects Limb Shortening 
Hirschsprung Disease Polydactyly Heart Disease 
Hirschsprung Disease with Heart Defects, Laryngeal Anomalies, and Preaxial Polydactyly 
Hirschsprung Disease with Polydactyly, Renal Agenesis, and Deafness 
Hirschsprung Disease with Ulnar Polydactyly, Polysyndactyly of Big Toes, and Ventricular Septal Defect 
holoprosencephaly 9  
hydrolethalus syndrome +   
hypochondroplasia  
Hypoglossia-Hypodactylia 
Hypoplasia of Tibia with Polydactyly  
hypoplastic or aplastic tibia with polydactyly  
Ichthyosis Tapered Fingers Midline Groove Up 
INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, SEIZURES, AND DISTAL LIMB ANOMALIES  
Kaplan Plauchu Fitch Syndrome 
Kaufman oculocerebrofacial syndrome  
Kozlowski-Krajewska Syndrome 
Kuster Syndrome 
Laryngeal Atresia, Encephalocele, and Limb Deformities 
Laurence Prosser Rocker Syndrome 
Le Marec Bracq Picaud Syndrome 
Limb-Mammary Syndrome  
Liver Fibrocystic Disease and Polydactyly 
Lower Extremity Deformities, Congenital +   
Lynch Lee Murday syndrome 
Malformation of Arms 
Maroteaux Fonfria Syndrome 
McKusick-Kaufman syndrome  
Meckel syndrome 13  
Meckel syndrome 4  
Meckel-Like Cerebrorenodigital Syndrome 
Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus Syndrome +   
Megalodactyly  
Mental Retardation Spasticity Ectrodactyly 
Mesomelia-Synostoses Syndrome 
Metaphyseal Anadysplasia +   
Mexican Cardiomelic Dysplasia 
Microphthalmia with Cyst, Bilateral Facial Clefts, and Limb Anomalies 
Microphthalmia, Syndromic 6  
Multiple Epiphyseal Dysplasia with Robin Phenotype 
Multiple Pterygium Syndrome, X-Linked 
Nephrosis Deafness Urinary Tract Digital Malformation 
Neu-Laxova syndrome 1  
NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND DISTAL SKELETAL ANOMALIES  
Nievergelt Syndrome 
Oliver Syndrome 
Palant Cleft Palate Syndrome 
Pallister-Hall syndrome +   
Penttinen-Aula Syndrome  
Peters plus syndrome  
Pfeiffer Mayer Syndrome 
Pointer Syndrome 
polydactyly +   
Polydactyly Myopia Syndrome 
postaxial acrofacial dysostosis  
Postaxial Polydactyly +   
Powell Chandra Saal Syndrome 
Preaxial Polydactyly +   
Proteus syndrome +   
Pseudotrisomy 13 Syndrome 
Radial Ray Deficiency, X-Linked 
Radiohumeral Fusions with Other Skeletal and Craniofacial Anomalies  
rapadilino syndrome  
Reardon Hall Slaney syndrome 
Renal Dysplasia - Limb Defects Syndrome 
Robinow syndrome +   
Ruzicka Goerz Anton syndrome 
Santos Mateus Leal Syndrome 
Santos Syndrome 
Short Stature-Obesity Syndrome 
Splenogonadal Fusion Limb Defects Micrognatia 
split hand-foot malformation +   
split hand-foot malformation 1  
split hand-foot malformation 1 with sensorineural hearing loss  
split hand-foot malformation 2 
split hand-foot malformation 3  
split hand-foot malformation 4  
split hand-foot malformation 5 
split hand-foot malformation 6  
SPLIT-FOOT MALFORMATION WITH MESOAXIAL POLYDACTYLY  
Split-Hand and Split-Foot With Hypodontia 
Split-Hand with Obstructive Uropathy, Spina Bifida, and Diaphragmatic Defects 
Split-Hand-Foot Malformation with Long Bone Deficiency 1 
Split-Hand/Foot Malformation with Long Bone Deficiency 2 
Split-Hand/Foot Malformation with Long Bone Deficiency 3 
Steinfeld Syndrome 
Stern Lubinsky Durrie Syndrome 
Stratton-Parker Syndrome 
syndactyly +   
Syndactyly, Type IV  
Syndactyly-Polydactyly-Earlobe Syndrome 
Synpolydactyly 2  
Synpolydactyly 3 
Synpolydactyly with Foot Anomalies  
Tetramelic Monodactyly 
Tetramelic Postaxial Oligodactyly 
Thai Symphalangism Syndrome 
thanatophoric dysplasia +   
Thoracic Dysplasia-Hydrocephalus Syndrome 
Thoraco Limb Dysplasia Rivera Type 
Thoracomelic Dysplasia 
Tibia Absent Polydactyly Arachnoid Cyst 
Tibia, Absence or Hypoplasia of, with Polydactyly, Retrocerebellar Arachnoid Cyst, and Other Anomalies 
Ulnar Hypoplasia with Mental Retardation 
Upper Extremity Deformities, Congenital +   
Urioste Martinez-Frias Syndrome 
VACTERL association  
Viljoen Kallis Voges Syndrome 
Weill-Marchesani Syndrome 3  
Weyers acrofacial dysostosis  
Wright Dyck Syndrome 
Yunis-Varon syndrome  

Synonyms
Exact Synonyms: SFMMP
Primary IDs: OMIM:616890
Alternate IDs: RDO:9001173

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.