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Ontology Browser

Term:
Tetra Amelia with Ectodermal Dysplasia and Lacrimal Duct Abnormalities (DOID:9004156)
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Parent Terms Term With Siblings Child Terms
Ectromelia +     
3MC syndrome 3  
Absence of Tibia +   
Abuse Dwarfism Syndrome 
Adams-Oliver syndrome +   
ADULT syndrome  
AGAT deficiency  
Al Awadi Syndrome  
Al Gazali Sabrinathan Nair Syndrome 
Alves Castelo dos Santos Syndrome 
Amelia and Terminal Transverse Hemimelia 
Amelia, Autosomal Recessive  
Anal Sphincter Dysplasia 
Anhidrotic Ectodermal Dysplasia with Immunodeficiency, Osteopetrosis, and Lymphedema  
ankyloblepharon-ectodermal defects-cleft lip/palate syndrome  
Aplasia Cutis Congenita of Limbs Recessive 
Aplasia Cutis Congenita with Epibulbar Dermoids  
Aplasia Cutis Congenita with Intestinal Lymphangiectasia 
Aplasia Cutis Congenita, Congenital Heart Defect, and Frontonasal Cysts 
Aplasia Cutis Congenita, High Myopia, and Cone-Rod Dysfunction 
AREDYLD Syndrome 
Arthrogryposis and Ectodermal Dysplasia 
Arthrogryposis, Cleft Palate, Craniosynostosis, and Impaired Intellectual Development  
Bagatelle Cassidy syndrome 
Bainbridge-Ropers Syndrome  
Basan Syndrome  
Beaulieu-Boycott-Innes Syndrome  
Bosch-Boonstra-Schaaf Optic Atrophy Syndrome  
Brachycephaly, Trichomegaly, and Developmental Delay  
Bresheck/Bresek Syndrome 
Brunoni Syndrome 
cardiofaciocutaneous syndrome +   
Cerebellar Ataxia Ectodermal Dysplasia 
Cerebellar Atrophy with Seizures and Variable Developmental Delay  
CEREBELLAR ATROPHY, DEVELOPMENTAL DELAY, AND SEIZURES  
Cerebellar Hypoplasia +   
Cerebellofaciodental Syndrome  
Charcot Marie Tooth Type 1 Aplasia Cutis Congenita 
Chitayat Moore Del Bigio Syndrome 
Chitty Hall Webb Syndrome 
Chondrodysplasia, Megarbane-Dagher-Melki Type  
chromosome 13q14 deletion syndrome  
chromosome 17p13.3 duplication syndrome  
chromosome 3q29 microdeletion syndrome 
chromosome Xp11.23-p11.22 duplication syndrome 
Cleft Lip with or without Cleft Palate, Nonsyndromic, 8 
cleft lip-palate-ectodermal dysplasia syndrome  
Clouston syndrome  
Cohen syndrome  
CONGENITAL CONTRACTURES OF THE LIMBS AND FACE, HYPOTONIA, AND DEVELOPMENTAL DELAY  
Congenital Ectodermal Dysplasia with Hearing Loss 
CONGENITAL HEART DEFECTS AND ECTODERMAL DYSPLASIA  
Congenital Heart Defects, Dysmorphic Facial Features, and Intellectual Developmental Disorder  
CONGENITAL HYPOTONIA, EPILEPSY, DEVELOPMENTAL DELAY, AND DIGITAL ANOMALIES  
Craniofacial Abnormalities, Cataracts, Congenital Heart Disease, Sacral Neural Tube Defects, and Growth and Developmental Retardation 
Deafness with Anhidrotic Ectodermal Dysplasia 
Der Kaloustian Mcintosh Silver Syndrome 
Dermatoosteolysis Kirghizian Type 
dermatopathia pigmentosa reticularis  
Desanto-Shinawi Syndrome  
DEVELOPMENTAL DELAY WITH OR WITHOUT DYSMORPHIC FACIES AND AUTISM  
DEVELOPMENTAL DELAY, INTELLECTUAL DISABILITY, OBESITY, AND DYSMORPHIC FEATURES  
Diencephalic-Mesencephalic Junction Dysplasia Syndrome 2  
DK Phocomelia Syndrome 
Dyskinesias, Seizures, and Intellectual Developmental Disorder  
ectodermal dysplasia 13  
ectodermal dysplasia 14  
ectodermal dysplasia 8 
Ectodermal Dysplasia Adrenal Cyst 
Ectodermal Dysplasia and Neurosensory Deafness 
Ectodermal Dysplasia Mental Retardation Syndactyly 
Ectodermal Dysplasia Syndrome with Distinctive Facial Appearance and Preaxial Polydactyly of Feet 
Ectodermal Dysplasia with Natal Teeth, Turnpenny Type 
Ectodermal Dysplasia, Alopecia, Preaxial Polydactyly 
ectodermal dysplasia, ectrodactyly, and macular dystrophy syndrome  
Ectodermal Dysplasia, Sensorineural Hearing Loss, and Distinctive Facial Features 
Ectodermal Dysplasia, Trichoodontoonychial Type 
Ectodermal Dysplasia-Skin Fragility Syndrome  
Ectodermal Dysplasia-Syndactyly Syndrome +   
ECTODERMAL DYSPLASIA/SHORT STATURE SYNDROME  
Ectrodactyly and Ectodermal Dysplasia without Cleft Lip/Palate 
ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 1 
ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 3  
EEC syndrome +   
Ellis-Van Creveld syndrome +   
Euhidrotic Ectodermal Dysplasia 
focal dermal hypoplasia +   
Forebrain Defects  
Forsythe-Wakeling Syndrome 
Fragile Site 16p12 
Freire-Maia Odontotrichomelic Syndrome 
Gillessen-Kaesbach-Nishimura Dysplasia  
GLOBAL DEVELOPMENTAL DELAY WITH OR WITHOUT IMPAIRED INTELLECTUAL DEVELOPMENT  
GLOBAL DEVELOPMENTAL DELAY, ABSENT OR HYPOPLASTIC CORPUS CALLOSUM, AND DYSMORPHIC FACIES  
Global Developmental Delay, Lung Cysts, Overgrowth, and Wilms Tumor  
Global Developmental Delay, Progressive Ataxia, and Elevated Glutamine  
Growth Retardation, Developmental Delay, Coarse Facies, and Early Death  
Grubben de Cock Borghgraef Syndrome 
Halal Setton Wang Syndrome 
Hay Wells Syndrome Recessive Type 
Heyn-Sproul-Jackson Syndrome  
Hidrotic Ectodermal Dysplasia, Autosomal Recessive 
Hidrotic Ectodermal Dysplasia, Christianson-Fourie Type 
hypermethioninemia due to adenosine kinase deficiency  
hypohidrotic ectodermal dysplasia +   
HYPOPIGMENTATION, ORGANOMEGALY, AND DELAYED MYELINATION AND DEVELOPMENT  
Hypoplasia of Tibia with Polydactyly  
HYPOTONIA, ATAXIA, AND DELAYED DEVELOPMENT SYNDROME  
HYPOTONIA, ATAXIA, DEVELOPMENTAL DELAY, AND TOOTH ENAMEL DEFECT SYNDROME  
IMMUNODEFICIENCY, DEVELOPMENTAL DELAY, AND HYPOHOMOCYSTEINEMIA  
Johanson-Blizzard syndrome  
Johnson Munson Syndrome 
Jones Hersh Yusk Syndrome 
junctional epidermolysis bullosa with pyloric atresia  
Kat6a Syndrome  
Keppen-Lubinsky Syndrome  
Ladda Zonana Ramer syndrome 
Lamb-Shaffer Syndrome  
Laurin-Sandrow syndrome  
Lelis Syndrome 
Linear Skin Defects with Multiple Congenital Anomalies 2  
Loucks-Innes Syndrome  
Luscan-Lumish syndrome  
Marshall syndrome +   
Microcephaly, Cataracts, Impaired Intellectual Development, and Dystonia with Abnormal Striatum  
Microcephaly, Growth Retardation, Cataract, Hearing Loss, and Unusual Appearance 
microcephaly, seizures, and developmental delay  
Midface Hypoplasia, Obesity, Developmental Delay, and Neonatal Hypotonia 
Mitochondrial Progressive Myopathy with Congenital Cataract, Hearing Loss, and Developmental Delay  
Naegeli-Franceschetti-Jadassohn syndrome  
NEMO Mutation with Immunodeficiency 
Neurocutaneous Syndromes +   
Non-Lissencephalic Cortical Dysplasia 
Obesity, Hyperphagia, and Developmental Delay  
Odontomicronychial Dysplasia 
Odontoonychodermal Dysplasia  
Odontotrichoungual-Digital-Palmar Syndrome 
Ogden syndrome  
Ohdo syndrome +   
Oliver-McFarlane syndrome  
orofacial cleft 7 +   
Osteosclerotic Metaphyseal Dysplasia  
PACHYGYRIA, MICROCEPHALY, DEVELOPMENTAL DELAY, AND DYSMORPHIC FACIES, WITH OR WITHOUT SEIZURES 
pachyonychia congenita +   
palmoplantar keratoderma and congenital alopecia 1  
palmoplantar keratoderma and congenital alopecia 2 
Papillon-Lefevre disease +   
Partington Anderson Syndrome 
Periventricular Nodular Heterotopia with Syndactyly, Cleft Palate and Developmental Delay  
Photosensitive Trichothiodystrophy 1  
Pierpont syndrome  
Pinheiro Freire-Maia Miranda Syndrome 
Pseudo-TORCH Syndrome +   
pure hair and nail ectodermal dysplasia +   
Rajab Syndrome  
Rapp-Hodgkin syndrome  
Refsum Disease with Increased Pipecolic Acidemia 
Rhizomelic Short Stature with Microcephaly, Micrognathia, and Developmental Delay  
Richieri Costa Da Silva Syndrome 
Roberts syndrome  
Robinson Miller Bensimon Syndrome 
Roifman-Chitayat Syndrome 
Rosselli-Gulienetti Syndrome 
Rudd Klimek Syndrome 
scalp-ear-nipple syndrome  
Schopf-Schulz-Passarge syndrome  
Selig Benacerraf Greene Syndrome 
Sener Syndrome 
Sensenbrenner syndrome +   
Seres-Santamaria Arimany Muniz Syndrome 
Short Stature, Developmental Delay, and Congenital Heart Defects  
SIDDIQI SYNDROME  
sideroblastic anemia with B-cell immunodeficiency, periodic fevers, and developmental delay  
SNIJDERS BLOK-FISHER SYNDROME  
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 
Stiff Thumbs, with Brachydactyly Type A1 and Developmental Delay 
succinic semialdehyde dehydrogenase deficiency  
Taurodontia Absent Teeth Sparse Hair 
Ter Haar Syndrome  
Tetra Amelia with Ectodermal Dysplasia and Lacrimal Duct Abnormalities 
Tetraamelia Multiple Malformations 
Tetraamelia Syndrome 1  
Tetraamelia Syndrome 2  
Tetraphocomelia-Thrombocytopenia Syndrome 
Trichodental Syndrome 
Trichoodontoonychial Dysplasia 
Trichoscyphodysplasia 
Trueb Burg Bottani Syndrome 
Turnpenny-Fry Syndrome  
Unilateral Radioulnar Synostosis with Developmental Retardation and Hypotonia 
VERVERI-BRADY SYNDROME  
WEISS-KRUSZKA SYNDROME  
X-Linked Tetra-Amelia 
Yim Ebbin Syndrome 
Yunis-Varon syndrome  

Synonyms
Exact Synonyms: Absence of all four limbs with ectodermal dysplasia and lacrimal duct abnormalities ;   Tetraamelia With Ectodermal Dysplasia And Lacrimal Duct Abnormalities
Primary IDs: MESH:C536496
Alternate IDs: OMIM:273390 ;   RDO:0002098

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