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Ontology Browser

Term:
Cenani-Lenz syndactyly syndrome (DOID:0090015)
Annotations: Rat: (1) Mouse: (1) Human: (2) Chinchilla: (1) Bonobo: (1) Dog: (1) Squirrel: (1) Pig: (1)
Parent Terms Term With Siblings Child Terms
dysostosis +     
genetic disease +     
syndactyly +     
Achard syndrome 
acrocephalosyndactylia +   
acrodysostosis +   
acrofacial dysostosis +   
acrofrontofacionasal dysostosis 
acromelic frontonasal dysostosis  
Adrenocortical Hypofunction, Chronic Primary Congenital 
adrenocorticotropic hormone deficiency  
advanced sleep phase syndrome 3  
age related macular degeneration 8  
Agenesis of Cervical Vertebrae 
Alagille syndrome  
Alpha-2-Deficient Collagen Disease 
Aphalangia Syndactyly Microcephaly 
Aquaporin 1 Deficiency 
ataxic cerebral palsy 
atrial heart septal defect 3  
atrial heart septal defect 4  
Aurocephalosyndactyly 
autoimmune lymphoproliferative syndrome +   
Autosomal Recessive Syndrome of Syndactyly, Undescended Testes and Central Nervous System Defects  
Blepharophimosis with Ptosis, Syndactyly, and Short Stature 
Bonneau Syndrome 
brachydactyly +   
brachydactyly type A1B 
brachydactyly type A1C  
brachydactyly type A1D  
brachydactyly type B1  
brachydactyly type B2  
brachydactyly type E1  
brachydactyly type E2  
brachydactyly-syndactyly syndrome  
CADASIL +   
CAKUT2  
Camptodactyly Joint Contractures and Facial Skeletal Dysplasia 
cataract 23  
cataract 25 
cataract 26 multiple types 
cataract 27  
cataract 28 
Cenani-Lenz syndactyly syndrome  
A dysostosis characterized by syndactyly, malformation of the forearm and lower limb bones, renal hypoplasia or aplasia and that has_material_basis_in homozygous or compound heterozygous mutation in the LRP4 gene on chromosome 11p11. (DO)
CHARGE syndrome  
chromosomal disease +   
cleft lip-palate-ectodermal dysplasia syndrome  
complex cortical dysplasia with other brain malformations 1  
complex cortical dysplasia with other brain malformations 2  
complex cortical dysplasia with other brain malformations 3  
complex cortical dysplasia with other brain malformations 4  
complex cortical dysplasia with other brain malformations 5  
complex cortical dysplasia with other brain malformations 6  
congenital heart defects, hamartomas of tongue, and polysyndactyly  
Congenital Hepatic Fibrosis  
Congenital Pain Insensitivity +   
Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndromes +   
Cousin Syndrome  
Crossed Polysyndactyly 
desquamative interstitial pneumonia  
Diaphanospondylodysostosis  
Duplication of Eyebrows with Stretchable Skin and Syndactyly 
Dwarfism +   
Ectodermal Dysplasia, Mental Retardation, Syndactyly 
Ectodermal Dysplasia-Syndactyly Syndrome +   
Familial Cirrhosis +   
Familial Dysalbuminemic Hyperthyroxinemia  
Familial Hemophagocytic Lymphohistiocytoses +   
familial hypertrophic cardiomyopathy +   
Familial Lipochrome Histiocytosis 
Familial Mixed Cryoglobulinemia  
Familial Temporal Epilepsy +   
Fibular Aplasia, Tibial Campomelia, and Oligosyndactyly Syndrome 
Filippi syndrome  
focal dermal hypoplasia +   
Fraser syndrome +   
Frints De Smet Fabry Fryns Syndrome 
Fronto-Facio-Nasal Dysplasia 
Frontonasal Dysplasia 1  
frontotemporal dementia and/or amyotrophic lateral sclerosis-3  
frontotemporal dementia and/or amyotrophic lateral sclerosis-4  
Genetic Skin Diseases +   
Gollop Coates Syndrome 
Grange Syndrome  
Green Sandford Davison Syndrome 
hereditary angioedema +   
Hereditary Bilateral Parotidomegaly 
Hereditary Epistaxis 
Hereditary Eye Diseases +   
hereditary lymphedema +   
Hereditary Neoplastic Syndromes +   
Humerofemoral Hypoplasia with Radiotibial Ray Deficiency  
hypogonadotropic hypogonadism 5 with or without anosmia +   
inherited metabolic disorder +   
Isolated Prolactin Deficiency 
Isolated Thoracic Dysostosis 
Kallmann syndrome +   
Kleiner Holmes Syndrome 
Klippel-Feil syndrome +   
Kozlowski-Krajewska Syndrome 
LADD syndrome  
Laminopathies +   
Landy Donnai Syndrome 
Laurin-Sandrow syndrome  
Lennox-Gastaut syndrome  
Mandibulofacial Dysostosis Syndrome, Bauru Type 
Mandibulofacial Dysostosis with Macroblepharon and Macrostomia 
Marfan syndrome +   
Martinez Monasterio Pinheiro Syndrome 
Mesoaxial Synostotic Syndactyly with Phalangeal Reduction  
Metaphyseal Dysostosis, Mental Retardation, and Conductive Deafness 
monogenic disease +   
Naguib-Richieri-Costa Syndrome 
Nervous System Heredodegenerative Disorders +   
Nonimmune Chronic Idiopathic Neutropenia, Adult  
oculodentodigital dysplasia +   
orofacial cleft 7 +   
orofaciodigital syndrome +   
osteochondrodysplasia +   
Pavone Fiumara Rizzo Syndrome 
Periventricular Nodular Heterotopia 7  
Pfeiffer Rockelein Syndrome 
Piepkorn Karp Hickok syndrome 
Poland syndrome 
polygenic disease +   
popliteal pterygium syndrome +   
Postaxial Polydactyly, Type A4 
primary hypertrophic osteoarthropathy +   
progressive familial intrahepatic cholestasis +   
Radio-Ulnar Synostosis Type 1 
Radio-Ulnar Synostosis Type 2 
Rosselli-Gulienetti Syndrome 
Rubinstein-Taybi syndrome +   
Sacral Agenesis with Vertebral Anomalies  
sclerosteosis +   
Short Stature, Facial Dysmorphism, Severe Brachydactyly, and Syndactyly 
spondylocostal dysostosis +   
Spondylospinal Thoracic Dysostosis 
Stapes Ankylosis with Broad Thumbs and Toes  
syndactyly type 1  
syndactyly type 3  
syndactyly type 4  
syndactyly type 5  
Syndactyly Type 6 
syndactyly type 8  
Syndactyly-Polydactyly-Earlobe Syndrome 
syndactyly-telecanthus-anogenital and renal malformations syndrome  
synostosis +   
synpolydactyly +   
tarsal-carpal coalition syndrome +   
Thoracopelvic Dysostosis 
Timothy syndrome  
Trueb Burg Bottani Syndrome 
Winter Shortland Temple Syndrome  
yellow nail syndrome +  
Zerres Rietschel Majewski Syndrome 
zygodactyly 1 

Synonyms
Exact Synonyms: CLSS ;   Cenani syndactylism ;   Cenani-Lenz Syndactyly ;   Syndactyly type 7 ;   syndactyly type VII ;   syndactyly, Cenani-Lenz type
Primary IDs: MESH:C538150
Alternate IDs: OMIM:212780
Xrefs: GARD:5084 ;   ORDO:3258
Definition Sources: https://www.ncbi.nlm.nih.gov/pubmed/18978656 "DO", https://www.ncbi.nlm.nih.gov/pubmed/20381006 "DO", https://www.ncbi.nlm.nih.gov/pubmed/6279340 "DO"

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