FTP Download
Chinchilla Research Resource Database
   
Keyword
  

Ontology Browser

Term:
Macroepiphyseal Dysplasia, McAlister Coe Type (DOID:9004445)
Annotations: Rat: (0) Mouse: (0) Human: (0) Chinchilla: (0) Bonobo: (0) Dog: (0) Squirrel: (0)
Parent Terms Term With Siblings Child Terms
osteoporosis +     
skin disease +     
Achenbach syndrome 
Acneiform Eruptions +   
Acro-Osteolysis +   
Acromicric Dysplasia +   
adiaspiromycosis 
Agonadism, XY, with Mental Retardation, Short Stature, Retarded Bone Age, and Multiple Extragenital Malformations 
allergic cutaneous vasculitis +   
Amino Aciduria with Mental Deficiency, Dwarfism, Muscular Dystrophy, Osteoporosis, and Acidosis 
ancylostomiasis +  
Angel Shaped Phalangoepiphyseal Dysplasia 
angioedema +   
Au-Kline Syndrome  
Baby Rattle Pelvis Dysplasia 
Battaglia Neri Syndrome 
Bazopoulou Kyrkanidou Syndrome 
Bellini Chiumello Rimoldi Syndrome 
Bent Bone Dysplasia Syndrome  
Blount's disease 
Bone Dysplasia, Lethal, Holmgren Type 
Boudhina Yedes Khiari syndrome 
Brachioskeletogenital Syndrome  
Brachymesomelia Renal Syndrome 
breast disease +   
Brittle Bone Disorder 
Camptodactyly, Fibrous Tissue Hyperplasia, and Skeletal Dysplasia 
camptodactyly-tall stature-scoliosis-hearing loss syndrome  
cercarial dermatitis 
Cervical Vertebral Dysplasia 
chancroid +  
CHOPS SYNDROME  
chronic ulcer of skin +   
clubfoot +   
coenurosis 
contagious pustular dermatitis 
Cortical Defects, Wormian Bones, and Dentinogenesis Imperfecta 
craniolenticulosutural dysplasia  
Cutaneous Fistula 
cutaneous lupus erythematosus +   
cutis laxa +   
Deafness Conductive Ptosis Skeletal Anomalies 
Dermal Fibrosis  
dermatitis +   
Dermatoleukodystrophy 
dermatomyositis +   
Diabetic Bone Disease 
Diaphragmatic Defects, Limb Deficiencies, and Ossification Defects Of Skull 
Diaphyseal Medullary Stenosis with Malignant Fibrous Histiocytoma  
dipetalonemiasis 
Doughnut Lesions of Skull, Familial 
Duplication of Eyebrows with Stretchable Skin and Syndactyly 
Dwarfism +   
dysostosis +   
Dysplasia Epiphysealis Hemimelica +  
Ectodermal Dysplasia-Skin Fragility Syndrome  
Eczematous Skin Diseases +   
Elastosis Perforans Serpiginosa 
Elliott Ludman Teebi Syndrome 
endometriosis in scar of skin 
epidermal nevus +   
epidermolytic hyperkeratosis +   
Erythema +   
erythematosquamous dermatosis 
EVEN-PLUS SYNDROME  
exanthem +   
FACES Syndrome 
facial dermatosis +   
Facial Ectodermal Dysplasia  
Female Athlete Triad Syndrome 
filariasis +   
Flynn Aird Syndrome 
Focal Facial Dermal Dysplasia 4  
Foot Diseases +   
Fountain Syndrome 
Fryns Hofkens Fabry Syndrome 
Fuhrmann syndrome  
Funnel Chest +   
Genetic Skin Diseases +   
Gigantism +   
Gillessen-Kaesbach-Nishimura Dysplasia  
glucocorticoid-induced osteoporosis 
Gorham's disease +  
Gracile Bone Dysplasia  
Growth Failure, Microcephaly, Mental Retardation, Cataracts, Large Joint Contractures, Osteoporosis, Cortical Dysplasia, and Cerebellar Atrophy 
Gurrieri Sammito Bellussi Syndrome 
hair disease +   
Hall Riggs Mental Retardation Syndrome 
hand dermatosis +  
hemorrhoid +   
Hernandez Fragoso Syndrome 
Hypophosphatemic Nephrolithiasis/Osteoporosis +   
ichthyosis +   
idiopathic juvenile osteoporosis  
Infantile Multisystem Neurologic Disease with Osseous Fragility 
Infectious Skin Diseases +   
Ischiopatellar Dysplasia  
juvenile xanthogranuloma 
Kantaputra Gorlin Syndrome 
KBG syndrome  
keratosis +   
Kimura disease 
Kozlowski Rafinski Klicharska Syndrome 
Kozlowski Warren Fisher Syndrome 
Kyphomelic Dysplasia 
leg dermatosis 
Leg Length Inequality 
Lenz Majewski Hyperostotic Dwarfism  
lipomatosis +   
Lissencephaly Type III and Bone Dysplasia 
localized scleroderma +   
loiasis 
Macroepiphyseal Dysplasia, McAlister Coe Type 
Marfan syndrome +   
Marfan Syndrome, Autosomal Recessive  
Marshall-Smith syndrome  
MASS Syndrome  
mastocytosis +   
Median Cleft Lip, Corpus Callosum, Lipoma, and Skin Polyps 
Membranous Cranial Ossification, Delayed 
Mental Retardation, Joint Hypermobility, and Skin Laxity, with or without Metabolic Abnormalities 
Mesomelic Dysplasia, Camera Type 
Mesomelic Limb Shortening and Bowing 
Metabolic Skin Diseases +   
Miura type epiphyseal chondrodysplasia  
mongolian spot 
Morgellons Disease 
multicentric reticulohistiocytosis 
multiple cutaneous and mucosal venous malformations  
nail disease +   
necrobiosis lipoidica 
Necrobiotic Disorders +  
Necrolytic Migratory Erythema 
Nephrogenic Fibrosing Dermopathy  
nevoid basal cell carcinoma syndrome +   
noninfectious dermatoses of eyelid +  
Opitz Trigonocephaly Syndrome  
osteochondrodysplasia +   
Osteofibrous Dysplasia  
Osteosclerosis with Ichthyosis and Premature Ovarian Failure 
otulipenia  
Papulosquamous Skin Diseases +   
Patterson Pseudoleprechaunism Syndrome 
Pectus Carinatum  
phaeohyphomycosis +  
photosensitivity disease +   
pigmentation disease +   
Platybasia +  
Pointer Syndrome 
Postmenopausal Osteoporosis  
Prader-Willi Habitus, Osteopenia, and Camptodactyly 
Premature Aging, Okamoto Type 
Prenatal Bowing 
Proteus syndrome +   
Prurigo  
Pruritus +   
Pseudoatrophoderma Colli 
Radius Absent Anogenital Anomalies 
reactive cutaneous fibrous lesion +  
Rhizomelic Dysplasia Patterson Lowry Type 
Rhizomelic Dysplasia, Scoliosis, and Retinitis Pigmentosa 
Rhizomelic Syndrome 
Roifman-Chitayat Syndrome 
rosacea +   
Roy Maroteaux Kremp Syndrome 
Santos Syndrome 
scalp dermatosis +   
sebaceous gland disease +   
Short Stature, Auditory Canal Atresia, Mandibular Hypoplasia, Skeletal Abnormalities  
SHORT STATURE, BRACHYDACTYLY, INTELLECTUAL DEVELOPMENTAL DISABILITY, AND SEIZURES  
SHORT STATURE, FACIAL DYSMORPHISM, AND SKELETAL ANOMALIES WITH OR WITHOUT CARDIAC ANOMALIES  
Shwachman-Diamond Syndrome 2  
Singleton Merten Syndrome +   
Skeletal Defects, Genital Hypoplasia, And Mental Retardation  
Skeletal Dysplasia And Progressive Central Nervous System Degeneration, Lethal 
Skeletal Dysplasia with Delayed Epiphyseal and Carpal Bone Ossification 
Skeletal Dysplasia, Rhizomelic, with Retinitis Pigmentosa 
Skin Abnormalities +   
skin atrophy 
Skin Neoplasms +   
skin sarcoidosis 
split hand-foot malformation +   
Spondyloepimetaphyseal Dysplasia, Aggrecan Type  
Spranger Schinzel Myers Syndrome 
Stoll Levy Francfort Syndrome 
strongyloidiasis  
sweat gland disease +   
systemic scleroderma +   
Ter Haar Syndrome  
Trichoodontoonychial Dysplasia 
tyrosinemia type II  
Ulnar Hypoplasia with Mental Retardation 
Upton Young Syndrome 
urticaria +   
vascular skin disease +   
Verheij Syndrome  
verruciform xanthoma of skin 
Vertebral Body Fusion Overgrowth 
vesiculobullous skin disease +   
Wegener's granulomatosis +   
Weismann Netter Syndrome 
Wiedemann Oldigs Oppermann Syndrome 
Winchester Syndrome  

Synonyms
Exact Synonyms: Macroepiphyseal Dysplasia with Osteoporosis, Wrinkled Skin, and Aged Appearance ;   McAlister Coe Whyte syndrome
Primary IDs: MESH:C537721 ;   RDO:0003610

paths to the root