Disease Browser
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Parent Node: Abnormalities, Multiple (D000015) | Parent Node: Hearing Loss (D034381) | Parent Node: Lacrimal Apparatus Diseases (D007766) | Parent Node: Syndactyly (D013576) | Parent Node: Tooth Abnormalities (D014071) | ..Starting node ..Lacrimoauriculodentodigital syndrome (C538132)
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Sister Nodes: | ..Ackerman syndrome (C538170)
| ..Anodontia (D000848) 29
| ..AREDYLD Syndrome (C537427)
| ..Blepharo-cheilo-dontic syndrome (C536188)
| ..Book Syndrome (C562993)
| ..Carabelli Anomaly of Maxillary Molar Teeth (C566175)
| ..Cleidocranial Dysplasia, Forme Fruste, Dental Anomalies Only (C563974)
| ..CODAS syndrome (C536434)
| ..CRANIOSYNOSTOSIS AND DENTAL ANOMALIES (OMIM:614188)
| ..Deafness, Congenital, and Onychodystrophy, Autosomal Dominant (C567274)
| ..Deafness, Congenital, with Inner Ear Agenesis, Microtia, and Microdontia (C565195)
| ..Dens in Dente (D003719) 1
| ..Dental Enamel Hypoplasia (D003744) 29
| ..Dentin Dysplasia (D003805) 3
| ..Dentinogenesis Imperfecta (D003811) 7
| ..Dermoodontodysplasia (C565103)
| ..Diastema (D003970) 1
| ..Euhidrotic ectodermal dysplasia (C535763)
| ..Facial Dysmorphism, Selective Tooth Agenesis, and Choroid Calcification (C567039)
| ..Faciocardiomelic Dysplasia, Lethal (C565578)
| ..Fused Teeth (D005671)
| ..Grubben de Cock Borghgraef syndrome (C537621)
| ..Hypoglossia-Hypodactylia (C566308)
| ..Iridogoniodysgenesis, dominant type (C535536)
| ..Kallmann Syndrome 2 with Selective Tooth Agenesis (C566948)
| ..KBG syndrome (C537015)
| ..Lacrimoauriculodentodigital syndrome (C538132)
| ..Larsen syndrome, dominant type (C537873)
| ..Nance-Horan syndrome (C538336)
| ..Oculodentodigital Dysplasia (C563160)
| ..Oculodentodigital Dysplasia, Autosomal Recessive (C567605)
| ..Oculotrichodysplasia (C564934)
| ..Odontodysplasia (D018126) 3
| ..Odontomicronychial dysplasia (C537741)
| ..Odontotrichoungual-Digital-Palmar Syndrome (C566598)
| ..Oroacral Syndrome, Verloes-Koulischer Type (C566374)
| ..Otodental Dysplasia (C563482)
| ..Polydactyly, Postaxial, with Dental and Vertebral Anomalies (C564880)
| ..Rodrigues blindness (C535865)
| ..Spondyloepimetaphyseal Dysplasia With Abnormal Dentition (C566644)
| ..Taurodontism (C536946)
| ..Taurodontism, microdontia, and dens invaginatus (C536947)
| ..Teeth noneruption of with maxillary hypoplasia and genu valgum (C536952)
| ..Teeth, Odd Shapes Of (C566076)
| ..Temtamy preaxial brachydactyly syndrome (C536958)
| ..TOOTH AGENESIS, SELECTIVE, 7 (OMIM:616724)
| ..TOOTH AGENESIS, SELECTIVE, 8 (OMIM:617073)
| ..TOOTH AGENESIS, SELECTIVE, 9 (OMIM:617275)
| ..Tooth, Supernumerary (D014096) 3
| ..Tricho-dento-osseous syndrome 1 (C536550)
| ..TRICHODENTOOSSEOUS SYNDROME (OMIM:190320)
| ..Weyers acrofacial dysostosis (C536695)
| ..Zazam Sheriff Phillips syndrome (C536723)
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Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD
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Term ID: | 6754 |
Name: | Lacrimoauriculodentodigital syndrome |
Definition: | |
Alternative IDs: | OMIM:149730 |
ParentIDs: | MESH:D000015|MESH:D007766|MESH:D013576|MESH:D014071|MESH:D034381 |
TreeNumbers: | C05.116.099.370.894.819/C538132 |C05.660.585.800/C538132 |C05.660.906.819/C538132 |C07.650.800/C538132 |C07.793.700/C538132 |C09.218.458.341/C538132 |C10.597.751.418.341/C538132 |C11.496/C538132 |C16.131.077/C538132 |C16.131.621.585.800/C538132 |C16.131.621.906.81 |
Synonyms: | LADD |LADD SYNDROME |Levy Hollister syndrome |Levy-Hollister Syndrome |
Slim Mappings: | Congenital abnormality|Ear-nose-throat disease|Eye disease|Mouth disease|Musculoskeletal disease|Nervous system disease|Signs and symptoms |
Reference: |
MedGen: C538132
MeSH: C538132
OMIM: 149730; MSeqDR : Genes: FGF10; FGFR2; FGFR3; | Phenotypes | | Disease Causing ClinVar Variants | | MSeqDR Portal | |
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