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Ontology Browser

Term:
Osteosclerosis with Ichthyosis and Fractures (DOID:9004711)
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Parent Terms Term With Siblings Child Terms
Bone Fractures +     
ichthyosis +     
osteosclerosis +     
Acquired Ichthyosis 
Ankle Fractures 
autosomal recessive congenital ichthyosis +   
Avulsion Fractures 
axial osteomalacia 
Axial Osteosclerosis 
bullous congenital ichthyosiform erythroderma  
Camptodactyly-Ichthyosis Syndrome 
Camurati-Engelmann disease +   
Cataract and Congenital Ichthyosis 
CHIME syndrome  
Chitty Hall Webb Syndrome 
clavicle fractures 
Closed Fractures  
Congenital Ichthyosis with Trichothiodystrophy +   
congenital myopathy 9A  
craniodiaphyseal dysplasia +   
Craniofacial Dysostosis with Diaphyseal Hyperplasia 
craniometaphyseal dysplasia +   
Deal Barratt Dillon Syndrome 
Distal Osteosclerosis 
Dykes Markes Harper Syndrome 
Dysosteosclerosis +   
epidermolytic hyperkeratosis +   
Femoral Fractures +   
fibula fractures 
finger fractures 
Forney Robinson Pascoe Syndrome  
Fracture Dislocation +  
Fractures, Comminuted 
Fractures, Compression 
Fractures, Multiple 
Grover's Disease 
HID Syndrome  
Humeral Fractures 
Hyperostosis Cranialis Interna  
hypomyelinating leukodystrophy 8  
Ichthyosis Cheek Eyebrow Syndrome 
Ichthyosis Exfoliativa 
Ichthyosis Hystrix +   
Ichthyosis Prematurity Syndrome  
Ichthyosis Tapered Fingers Midline Groove Up 
ichthyosis vulgaris +   
Ichthyosis with Erythrokeratoderma  
ichthyosis, leukocyte vacuoles, alopecia, and sclerosing cholangitis  
Ichthyosis, Mental Retardation, Dwarfism, and Renal Impairment 
Ichthyosis, Spastic Quadriplegia, and Mental Retardation  
Ichthyosis, Split Hairs, and Amino Aciduria 
Ichthyosis-Mental Retardation Syndrome with Large Keratohyalin Granules in the Skin 
ICHTHYOTIC KERATODERMA, SPASTICITY, HYPOMYELINATION, AND DYSMORPHIC FACIAL FEATURES  
IFAP Syndrome +   
Infantile Multisystem Neurologic Disease with Osseous Fragility 
Intra-Articular Fractures 
Jagell Holmgren Hofer Syndrome 
Keratitis-Ichthyosis-Deafness Syndrome +   
Keratoderma-Ichthyosis-Deafness Syndrome, Autosomal Recessive  
keratosis pilaris atrophicans +   
knee fractures 
Koone Rizzo Elias Syndrome 
Lamellar Ichthyosis, Autosomal Dominant Form  
Lethal Osteosclerotic Chondrodysplasia, with Intracellular Inclusions 
Malunited Fractures 
melorheostosis +   
Mixed Sclerosing Bone Dystrophy 
Neu-Laxova syndrome 1  
Open Fractures 
osteopathia striata with cranial sclerosis  
osteopetrosis +   
Osteopoikilosis +   
Osteoporotic Fractures  
Osteosclerosis with Ichthyosis and Fractures 
osteosclerotic metaphyseal dysplasia  
Periprosthetic Fractures 
Pyknoachondrogenesis 
Radius Fractures +  
Raine Syndrome  
Rib Fractures  
Rud Syndrome 
Ruzicka Goerz Anton syndrome 
Sammartino De Crecchio Syndrome 
Shoulder Fractures +  
Sjogren-Larsson syndrome +   
Skull Fractures +   
Spinal Fractures  
Spinal Muscular Atrophy with Congenital Bone Fractures +   
spondyloepimetaphyseal dysplasia with joint laxity +   
Spontaneous Fractures  
Stormorken syndrome  
Stress Fractures  
Tibial Fractures +   
Trichodysplasia-Xeroderma 
Ulna Fractures +  
Ununited Fractures +   
Whyte Murphy Syndrome 
Worth syndrome  
wrist fractures 
X-linked ichthyosis +   
xeroderma of eyelid 

Synonyms
Exact Synonyms: Cortical Thickening of Long Bones with Bowing and Ichthyosis
Primary IDs: MESH:C563483
Alternate IDs: OMIM:166740

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