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Term:
Deafness with Anhidrotic Ectodermal Dysplasia (DOID:9002175)
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Parent Terms Term With Siblings Child Terms
Deafness +     
3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome  
Absence of Tibia with Congenital Deafness 
ACCES Syndrome  
Adams-Oliver syndrome +   
ADULT syndrome  
Albinism Deafness Syndrome 
Alves Castelo dos Santos Syndrome 
Anal Sphincter Dysplasia  
ankyloblepharon-ectodermal defects-cleft lip/palate syndrome  
Aplasia Cutis Congenita of Limbs Recessive 
Aplasia Cutis Congenita with Intestinal Lymphangiectasia 
Aplasia Cutis Congenita, Congenital Heart Defect, and Frontonasal Cysts 
Aplasia Cutis Congenita, High Myopia, and Cone-Rod Dysfunction 
APLASIA CUTIS-ENAMEL DYSPLASIA SYNDROME 
AREDYLD Syndrome 
Arthrogryposis and Ectodermal Dysplasia  
Arthrogryposis Multiplex with Deafness, Inguinal Hernias, and Early Death 
autosomal dominant congenital deafness with onychodystrophy  
autosomal dominant nonsyndromic deafness 65  
Ayazi Syndrome 
BASAN syndrome  
Branchiogenic-Deafness Syndrome 
Bresheck/Bresek Syndrome 
Brunoni Syndrome 
Burn-McKeown syndrome  
Cardioauditory Syndrome of Sanchez Cascos 
cardiofaciocutaneous syndrome +   
cartilage-hair hypoplasia  
Cerebellar Ataxia and Ectodermal Dysplasia 
Charcot Marie Tooth Type 1 Aplasia Cutis Congenita 
Cleft Lip with or without Cleft Palate, Nonsyndromic, 8  
cleft lip-palate-ectodermal dysplasia syndrome  
Clouston syndrome  
COLOBOMA, OSTEOPETROSIS, MICROPHTHALMIA, MACROCEPHALY, ALBINISM, AND DEAFNESS  
Congenital Deafness and Familial Myoclonic Epilepsy 
Congenital Deafness, with Vitiligo and Achalasia 
Congenital Ectodermal Dysplasia with Hearing Loss 
Congenital Emphysema, with Deafness, Penoscrotal Web, and Mental Retardation 
CONGENITAL HEART DEFECTS AND ECTODERMAL DYSPLASIA  
Congenital Myopathy with Neuropathy and Deafness  
Coxoauricular Syndrome 
cranioectodermal dysplasia +   
Davenport Donlan Syndrome 
Deaf-Blind Disorders +   
Deafness Hyperuricemia Neurologic Ataxia 
Deafness with Anhidrotic Ectodermal Dysplasia 
Deafness, Autosomal Dominant, due to Mutation In Myo1a 
DEAFNESS, CATARACT, IMPAIRED INTELLECTUAL DEVELOPMENT, AND POLYNEUROPATHY  
Deafness, Cataract, Retinitis Pigmentosa, And Sperm Abnormalities 
Deafness, Congenital Onychodystrophy, Recessive Form 
DEAFNESS, CONGENITAL, AND ADULT-ONSET PROGRESSIVE LEUKOENCEPHALOPATHY  
Deafness, with Smith-Magenis Syndrome  
Dermatoosteolysis Kirghizian Type 
dermatopathia pigmentosa reticularis  
Dislocated Elbows, Bowed Tibias, Scoliosis, Deafness, Cataract, Microcephaly, and Mental Retardation 
ectodermal dysplasia 13  
ectodermal dysplasia 14  
ectodermal dysplasia 8 
Ectodermal Dysplasia Adrenal Cyst 
Ectodermal Dysplasia and Neurosensory Deafness 
Ectodermal Dysplasia Syndrome with Distinctive Facial Appearance and Preaxial Polydactyly of Feet 
ECTODERMAL DYSPLASIA WITH FACIAL DYSMORPHISM AND ACRAL, OCULAR, AND BRAIN ANOMALIES  
Ectodermal Dysplasia with Natal Teeth, Turnpenny Type 
Ectodermal Dysplasia, Alopecia, Preaxial Polydactyly 
ectodermal dysplasia, ectrodactyly, and macular dystrophy syndrome  
Ectodermal Dysplasia, Mental Retardation, Syndactyly 
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 
EEC syndrome +   
Ellis-Van Creveld syndrome +   
Epiphyseal Dysplasia of Femoral Head, Myopia, and Deafness 
Euhidrotic Ectodermal Dysplasia 
Fine-Lubinsky Syndrome  
focal dermal hypoplasia  
Focal Facial Dermal Dysplasia +   
Fountain Syndrome 
Freire-Maia Odontotrichomelic Syndrome 
Halal Setton Wang Syndrome 
Hay Wells Syndrome Recessive Type 
hereditary spastic paraplegia 24 
Herrmann Syndrome 
Hidrotic Ectodermal Dysplasia, Autosomal Recessive 
Hidrotic Ectodermal Dysplasia, Christianson-Fourie Type 
high myopia-sensorineural deafness syndrome  
Hirschsprung Disease with Polydactyly, Renal Agenesis, and Deafness 
Hyperlipoproteinemia Type II, and Deafness 
HYPERTELORISM, PREAURICULAR SINUS, PUNCTAL PITS, AND DEAFNESS 
hypohidrotic ectodermal dysplasia +   
Hypokalemic Tubulopathy and Deafness  
ITM2B-related cerebral amyloid angiopathy 2  
Johanson-Blizzard syndrome  
Johnson Neuroectodermal Syndrome 
Jones Hersh Yusk Syndrome 
Jones Syndrome 
junctional epidermolysis bullosa with pyloric atresia  
Keipert syndrome  
Keratitis-Ichthyosis-Deafness Syndrome +   
Konigsmark Knox Hussels Syndrome 
Ladda Zonana Ramer Syndrome 
Lelis Syndrome 
LEUKOENCEPHALOPATHY, PROGRESSIVE, INFANTILE-ONSET, WITH OR WITHOUT DEAFNESS  
linear skin defects with multiple congenital anomalies 2  
Lynch Lee Murday syndrome 
Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome  
Marshall syndrome +   
Meyenburg-Altherr-Uehlinger Syndrome 
Microcephaly Deafness Syndrome 
Muckle-Wells syndrome  
multiple synostoses syndrome 1  
Myoclonic Epilepsy, Congenital Deafness, Macular Dystrophy, and Psychiatric Disorders 
Myoclonus, Cerebellar Ataxia, and Deafness 
Naegeli-Franceschetti-Jadassohn syndrome  
Nathalie Syndrome 
NEMO Mutation with Immunodeficiency 
Nephrosis with Deafness and Urinary Tract and Digital Malformations 
Neurocutaneous Syndromes +   
Noninsulin-Dependent Diabetes Mellitus with Deafness  
nonsyndromic aplasia cutis congenita  
nonsyndromic deafness +   
oculoectodermal syndrome  
Odontomicronychial Dysplasia 
Odontoonychodermal Dysplasia  
Odontotrichoungual-Digital-Palmar Syndrome 
Ohdo syndrome +   
Opticocochleodentate Degeneration 
orofacial cleft 7 +   
pachyonychia congenita +   
palmoplantar keratoderma and congenital alopecia 1  
palmoplantar keratoderma and congenital alopecia 2 
Papillon-Lefevre disease +   
Perrault syndrome +   
photosensitive trichothiodystrophy 1  
Pinheiro Freire-Maia Miranda Syndrome 
pure hair and nail ectodermal dysplasia +   
Ramos Arroyo Clark Syndrome 
Rapp-Hodgkin syndrome  
Ribbonlike Corneal Degeneration with Deafness 
Richards-Rundle Syndrome 
Robinson Miller Bensimon Syndrome 
Rosselli-Gulienetti Syndrome 
scalp-ear-nipple syndrome  
Schimke X-Linked Mental Retardation Syndrome 
Schinzel Giedion syndrome  
Schlegelberger Grote Syndrome 
Schopf-Schulz-Passarge syndrome  
Secretory Diarrhea, Myopathy, and Deafness 
Sener Syndrome 
Seres-Santamaria Arimany Muniz Syndrome 
Siddiqi syndrome  
Sinoatrial Node Dysfunction and Deafness  
spastic paraplegia with deafness 
Taurodontia, Absent Teeth, Sparse Hair 
temtamy preaxial brachydactyly syndrome  
Tetra Amelia with Ectodermal Dysplasia and Lacrimal Duct Abnormalities 
Tietz syndrome  
Trichodental Syndrome 
Trichoodontoonychial Dysplasia 
Trichoscyphodysplasia 
Trueb Burg Bottani Syndrome 
Wright Dyck Syndrome 
X-linked Alport syndrome  
X-linked mental retardation Gustavson type  
X-linked mental retardation-hypotonic facies syndrome-1  
X-linked retinitis pigmentosa and sinorespiratory infections  
Yemenite Deaf-Blind Hypopigmentation Syndrome 
Yunis-Varon syndrome  

Synonyms
Primary IDs: MESH:C565119
Alternate IDs: MIM:125050

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