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Ontology Browser

Term:
Dermatoosteolysis Kirghizian Type (DOID:9007678)
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Parent Terms Term With Siblings Child Terms
anodontia +     
keratitis +     
Osteolysis +     
Acanthamoeba Keratitis  
Acro-Osteolysis +   
Adams-Oliver syndrome +   
ADULT syndrome  
Aloi Tomasini Isaia Syndrome 
Alves Castelo dos Santos Syndrome 
Anal Sphincter Dysplasia 
Anhidrotic Ectodermal Dysplasia with Immunodeficiency, Osteopetrosis, and Lymphedema  
ankyloblepharon-ectodermal defects-cleft lip/palate syndrome  
Anodontia of Permanent Dentition 
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 
AREDYLD Syndrome 
Arthrogryposis and Ectodermal Dysplasia 
autosomal dominant keratitis +   
Axenfeld-Rieger syndrome type 1  
Axenfeld-Rieger syndrome type 2 
Bacterial Keratitis +   
Basan Syndrome  
Brachymetapody-Anodontia-Hypotrichosis-Albinoidism 
Bresheck/Bresek Syndrome 
Brunoni Syndrome 
Buruli ulcer disease  
cardiofaciocutaneous syndrome +   
cartilage-hair hypoplasia  
Cerebellar Ataxia 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  
Cleft Palate, Deafness, and Oligodontia 
Clouston syndrome  
Congenital Ectodermal Dysplasia with Hearing Loss 
CONGENITAL HEART DEFECTS AND ECTODERMAL DYSPLASIA  
corneal neovascularization +   
corneal ulcer +   
Deafness Oligodontia Syndrome 
Deafness with Anhidrotic Ectodermal Dysplasia 
decubitus ulcer  
deep keratitis +  
Dermatoosteolysis Kirghizian Type 
dermatopathia pigmentosa reticularis  
Dilated Cardiomyopathy with Woolly Hair, Keratoderma, and Tooth Agenesis  
Dysmyelinating Leukodystrophy with Oligodontia 
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 +   
Epidermolysis Bullosa, Late-Onset Localized Junctional, with Mental Retardation 
Euhidrotic Ectodermal Dysplasia 
familial expansile osteolysis  
filamentary keratitis 
focal dermal hypoplasia +   
Freire-Maia Odontotrichomelic Syndrome 
Fungal Keratitis  
gonococcal keratitis 
Gorham's disease +  
Growth Retardation, Alopecia, Pseudoanodontia and Optic Atrophy  
Halal Setton Wang Syndrome 
Hay Wells Syndrome Recessive Type 
herpes simplex virus keratitis +   
Hidrotic Ectodermal Dysplasia, Autosomal Recessive 
Hidrotic Ectodermal Dysplasia, Christianson-Fourie Type 
Hypodontia Oligodontia with Orofacial Cleft 
hypohidrotic ectodermal dysplasia +   
hypomyelinating leukodystrophy 7 with or without oligodontia and-or hypogonadotropic hypogonadism  
Hypotrichosis-Osteolysis-Periodontitis-Palmoplantar Keratoderma Syndrome 
Johanson-Blizzard syndrome  
Jones Hersh Yusk Syndrome 
junctional epidermolysis bullosa with pyloric atresia  
Keratitis Fugax Hereditaria  
Keratitis-Ichthyosis-Deafness Syndrome  
keratoconjunctivitis +   
Keratouveitis 
Ladda Zonana Ramer syndrome 
Lelis Syndrome 
Leukomelanoderma, Infantilism, Mental Retardation, Hypodontia, Hypotrichosis 
Linear Skin Defects with Multiple Congenital Anomalies 2  
macular keratitis 
Marshall syndrome +   
Mehta Lewis Patton Syndrome 
Microdontia Hypodontia Short Stature 
Naegeli-Franceschetti-Jadassohn syndrome  
NEMO Mutation with Immunodeficiency 
Nestor-Guillermo Progeria Syndrome  
Neurocutaneous Syndromes +   
oculoectodermal syndrome  
Odontomicronychial Dysplasia 
Odontoonychodermal Dysplasia  
Odontotrichoungual-Digital-Palmar Syndrome 
Ohdo syndrome +   
Oligodontia-Colorectal Cancer Syndrome  
orofacial cleft 7 +   
Osebold Skeletal Dysplasia Osteolysis Syndrome 
Osteolysis Hereditary Multicentric +   
Osteolysis Syndrome, Recessive 
pachyonychia congenita +   
palmoplantar keratoderma and congenital alopecia 1  
palmoplantar keratoderma and congenital alopecia 2 
Papillon-Lefevre disease +   
photokeratitis 
Photosensitive Trichothiodystrophy 1  
Pinheiro Freire-Maia Miranda Syndrome 
Polyosteolysis-Hyperostosis Syndrome 
pure hair and nail ectodermal dysplasia +   
pyoderma gangrenosum +   
Rapp-Hodgkin syndrome  
Robinson Miller Bensimon Syndrome 
Rosselli-Gulienetti Syndrome 
scalp-ear-nipple syndrome  
Schopf-Schulz-Passarge syndrome  
Sener Syndrome 
Sensenbrenner syndrome +   
Seres-Santamaria Arimany Muniz Syndrome 
solitary median maxillary central incisor  
Split-Hand and Split-Foot With Hypodontia 
superficial keratitis +  
Talo-Patello-Scaphoid Osteolysis, Synovitis, and Short Fourth Metacarpals 
Taurodontia Absent Teeth Sparse Hair 
Tetra Amelia with Ectodermal Dysplasia and Lacrimal Duct Abnormalities 
Thai Symphalangism Syndrome 
Thumb Deformity, Alopecia, Pigmentation Anomaly 
tooth and nail syndrome  
Trichodental Syndrome 
Trichoodontoonychial Dysplasia 
Trichoscyphodysplasia 
Trueb Burg Bottani Syndrome 
ulcer of lower limbs +   
Winchester Syndrome  
X-Linked Hypodontia 
Yunis-Varon syndrome  
Zadik Barak Levin Syndrome 

Synonyms
Exact Synonyms: Kirghizian dermatoosteolysis
Primary IDs: MESH:C535373
Alternate IDs: OMIM:221810

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