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Term:
Progressive Osseous Heteroplasia (DOID:9002436)
Annotations: Rat: (6) Mouse: (6) Human: (6) Chinchilla: (5) Bonobo: (6) Dog: (6) Squirrel: (6)
Parent Terms Term With Siblings Child Terms
Absence of Fingerprints  
Actinic Prurigo  
Albinism +   
Aloi Tomasini Isaia Syndrome 
Annular Erythema 
arterial tortuosity syndrome  
atopic dermatitis +   
Atrophia Maculosa Varioliformis Cutis, Familial 
AUTOINFLAMMATION WITH ARTHRITIS AND DYSKERATOSIS  
autosomal recessive congenital ichthyosis +   
Basaloid Follicular Hamartoma Syndrome, Generalized, Autosomal Dominant 
Bloch-Sulzberger syndrome +   
Bone Demineralization, Pathologic +  
bullous congenital ichthyosiform erythroderma  
Buschke-Ollendorff Syndrome  
Chitty Hall Baraitser Syndrome 
Collagenosis, Familial Reactive Perforating 
congenital disorder of glycosylation type IIa  
Congenital Erythroderma with Palmoplantar Keratoderma, Hypotrichosis, and Hyper-IgE  
Cutaneous Bullous Amyloidosis 
cutaneous porphyria  
cutis laxa +   
Desbuquois dysplasia +   
Dowling-Degos disease +   
dyschromatosis universalis hereditaria +   
dyskeratosis congenita +   
Eagle Syndrome 
ectodermal dysplasia +   
Ehlers-Danlos syndrome +   
epidermolysis bullosa +   
erythrokeratodermia variabilis +   
Erythrokeratodermia with Ataxia  
Exfoliative Ichthyosis, Autosomal Recessive, Ichthyosis Bullosa of Siemens-like  
Follicular Atrophoderma, Perioral Pigmented, with Milia and Epidermoid Cysts 
Gerodermia Osteodysplastica  
glycoproteinosis +   
Hailey-Hailey disease  
Hepatic Porphyrias +   
Hereditary Autoinflammatory Diseases +   
hereditary mucosal leukokeratosis  
Histiocytic Dermatoarthritis 
Hyaluronan Metabolism, Defect in 
Hypophosphatemic Bone Disease 
Hypouricemia, Hypercalcinuria, and Decreased Bone Density 
ichthyosis vulgaris +   
Isolated Osteopoikilosis 
Juvenile Spring Eruption of Ears 
Kaler Garrity Stern Syndrome 
Keratolytic Winter Erythema  
keratosis follicularis +   
Keratosis Follicularis Spinulosa Decalvans, X-Linked  
Keratosis Linearis with Ichthyosis Congenita and Sclerosing Keratoderma  
Leri Pleonosteosis 
Leukomelanoderma, Infantilism, Mental Retardation, Hypodontia, Hypotrichosis 
lipoid proteinosis  
monilethrix +   
Muir-Torre syndrome  
Multiple Noduli Cutanei with Urinary Tract Abnormalities 
Oculotrichodysplasia 
orofaciodigital syndrome IX  
Ossification of Posterior Longitudinal Ligament +   
osteoporosis +   
palmoplantar keratosis +   
Panostotic Fibrous Dysplasia 
Parana Hard Skin Syndrome 
Pedal Onychogryposis with Keratosis Plantaris and Coarse Hair 
peeling skin syndrome +   
Perifolliculitis Capitis Abscedens Et Suffodiens, Familial 
Plasminogen Deficiency, Type I  
Poikiloderma, Hereditary Sclerosing +   
porokeratosis +   
primary cutaneous amyloidosis  
Primary Localized Cutaneous Amyloidosis, 2  
Primary Localized Cutaneous Amyloidosis, 3  
Progressive Osseous Heteroplasia  
Progressive Vitiligo with Mental Retardation and Urethral Duplication 
Prolidase Deficiency  
pseudohypoparathyroidism +   
pseudoxanthoma elasticum +   
Reticulate Pigmentary Disorder, with Systemic Manifestations  
Revesz syndrome  
rickets +   
Rothmund-Thomson syndrome +   
Sjogren-Larsson syndrome +   
Skin Fragility-Woolly Hair Syndrome  
Stiff Skin Syndrome  
Storm Syndrome 
Superior Transverse Scapular Ligament, Calcification Of, Familial 
Systemic Hyalinosis  
Trichothiodystrophy Syndromes +   
Vohwinkel Syndrome, Variant Form  
X-linked ichthyosis +   
xeroderma pigmentosum +   

Synonyms
Exact Synonyms: Cutaneous Ossification ;   Ectopic Ossification, Familial ;   Osteodermia ;   Osteoma Cutis ;   Osteosis Cutis ;   POH
Primary IDs: MESH:C562735
Alternate IDs: OMIM:166350 ;   RDO:0012322

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