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Ontology Browser
Term:
Osteosclerosis with Ichthyosis and Fractures
(DOID:9004711)
Annotations:
Rat: (0)
Mouse: (0)
Human: (0)
Chinchilla: (0)
Bonobo: (0)
Dog: (0)
Squirrel: (0)
Pig: (0)
Naked Mole-rat: (0)
Green Monkey: (0)
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