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Term:
Gerodermia Osteodysplastica (DOID:9005031)
Annotations: Rat: (1) Mouse: (1) Human: (2) Chinchilla: (1) Bonobo: (1) Dog: (1) Squirrel: (1)
Parent Terms Term With Siblings Child Terms
bone disease +     
Dwarfism +     
3-M syndrome +   
Aarskog syndrome +   
Absence of Fingerprints  
Abuse Dwarfism Syndrome 
achondroplasia +   
acromesomelic dysplasia +   
Actinic Prurigo  
Alaninuria with Microcephaly, Dwarfism, Enamel Hypoplasia, and Diabetes Mellitus 
Albinism +   
Alopecia Contractures Dwarfism Mental Retardation 
Amino Aciduria with Mental Deficiency, Dwarfism, Muscular Dystrophy, Osteoporosis, and Acidosis 
anauxetic dysplasia 1  
Anauxetic Dysplasia 2  
Annular Erythema 
arterial tortuosity syndrome  
Astley-Kendall Syndrome 
Asymmetric Short Stature Syndrome 
Atelosteogenesis Type 3  
atopic dermatitis +   
Atrophia Maculosa Varioliformis Cutis, Familial 
AUTOINFLAMMATION WITH ARTHRITIS AND DYSKERATOSIS  
autosomal recessive congenital ichthyosis +   
Bangstad Syndrome 
Basaloid Follicular Hamartoma Syndrome, Generalized, Autosomal Dominant 
bejel 
Bird Headed Dwarfism Montreal Type 
Bloch-Sulzberger syndrome +   
bone benign neoplasm +   
Bone Cysts +   
bone development disease +   
bone inflammation disease +   
Bone Malalignment +   
Bone Neoplasms +   
bone remodeling disease +   
bone resorption disease +   
bone structure disease +   
Boomerang dysplasia  
Brachydactylous Dwarfism Mseleni Type 
Brachymetapody-Anodontia-Hypotrichosis-Albinoidism 
Brunoni Syndrome 
bullous congenital ichthyosiform erythroderma  
Bullous Dystrophy, Hereditary Macular Type 
Buschke-Ollendorff Syndrome  
Cantu Sanchez-Corona Fragoso Syndrome 
Chondrodysplasia Calcificans Metaphysealis 
Chondrodysplasia, Megarbane-Dagher-Melki Type  
chronic granulomatous disease +   
Cloverleaf Skull Micromelia Thoracic Dysplasia 
Cockayne syndrome +   
Collagenosis, Familial Reactive Perforating 
Congenital Erythroderma with Palmoplantar Keratoderma, Hypotrichosis, and Hyper-IgE  
congenital hypothyroidism +   
Coxa Magna 
Coxa Valga 
Cutaneous Bullous Amyloidosis 
cutaneous porphyria  
cutis laxa +   
cystic echinococcosis 
De Sanctis-Cacchione Syndrome  
Desbuquois dysplasia +   
diastrophic dysplasia  
Diastrophic Dysplasia, Broad Bone-Platyspondylic Variant  
Disproportionate Short Stature with Ptosis and Valvular Heart Lesions 
Dowling-Degos disease +   
Dwarfism Stiff Joint Ocular Abnormalities 
Dwarfism Tall Vertebrae 
Dwarfism, Familial, with Muscle Spasms 
Dwarfism, Levi Type 
Dwarfism, Low-Birth-Weight Type, with Unresponsiveness to Growth Hormone 
Dyggve-Melchior-Clausen disease +   
dyschromatosis universalis hereditaria +   
dyskeratosis congenita +   
Dyssegmental Dysplasia with Glaucoma 
ectodermal dysplasia +   
ECTODERMAL DYSPLASIA/SHORT STATURE SYNDROME  
Ehlers-Danlos syndrome +   
Endocrine Bone Diseases +   
Eosinophilic Granuloma 
epidermolysis bullosa +   
Epiphyses, Slipped +  
erythrokeratodermia variabilis +   
Erythrokeratodermia with Ataxia  
Exfoliative Ichthyosis, Autosomal Recessive, Ichthyosis Bullosa of Siemens-like  
Expansile Bone Lesions 
fibrochondrogenesis +   
Follicular Atrophoderma, Perioral Pigmented, with Milia and Epidermoid Cysts 
Genu Valgum +   
Genu Varum +   
Gerodermia Osteodysplastica  
Growth Retardation, Developmental Delay, Coarse Facies, and Early Death  
Hadziselimovic Syndrome 
Hailey-Hailey disease  
Hepatic Porphyrias +   
Hereditary Autoinflammatory Diseases +   
hereditary mucosal leukokeratosis  
Histiocytic Dermatoarthritis 
Ho Kaufman Mcalister Syndrome 
Hyaluronan Metabolism, Defect in 
Hypertelorism, Severe, with Midface Prominence, Myopia, Mental Retardation, and Bone Fragility  
hypochondroplasia  
hypohidrotic ectodermal dysplasia +   
ichthyosis vulgaris +   
Ichthyosis, Mental Retardation, Dwarfism, and Renal Impairment 
IMMUNOSKELETAL DYSPLASIA WITH NEURODEVELOPMENTAL ABNORMALITIES  
Infectious Bone Diseases +   
Intellectual Developmental Disorder with Abnormal Behavior, Microcephaly, and Short Stature  
ischemic bone disease +   
isolated growth hormone deficiency +   
Isolated Osteopoikilosis 
Joint Dislocations +   
Juvenile Spring Eruption of Ears 
Kennerknecht Vogel Syndrome 
Kenny-Caffey Syndrome, Type 2  
Keratolytic Winter Erythema  
keratosis follicularis +   
Keratosis Follicularis Dwarfism Cerebral Atrophy 
Keratosis Follicularis Spinulosa Decalvans, X-Linked  
Keratosis Linearis with Ichthyosis Congenita and Sclerosing Keratoderma  
Kniest dysplasia  
Laplane Fontaine Lagardere Syndrome 
Laron syndrome +   
Leukomelanoderma, Infantilism, Mental Retardation, Hypodontia, Hypotrichosis 
lipoid proteinosis  
Loucks-Innes Syndrome  
Mental Retardation, Macrocephaly, Short Stature and Craniofacial Dysmorphism 
Mental Retardation, Short Stature, Facial Anomalies, and Joint Dislocations 
Mesomelic Dwarfism of Hypoplastic Tibia and Radius Type 
Mesomelic Dwarfism Reinhardt Pfeiffer Type 
Metabolic Bone Diseases +   
Metatropic Dwarfism  
Metatropic Dwarfism, Type II 
Microcephalic Osteodysplastic Primordial Dwarfism +   
Microcephalic Primordial Dwarfism Toriello Type 
MICROCEPHALY, SHORT STATURE, AND IMPAIRED GLUCOSE METABOLISM +   
MICROCEPHALY, SHORT STATURE, AND POLYMICROGYRIA WITH OR WITHOUT SEIZURES  
Mollica Pavone Antener Syndrome 
monilethrix +   
Muir-Torre syndrome  
mulibrey nanism  
Multiple Noduli Cutanei with Urinary Tract Abnormalities 
Nievergelt Syndrome 
Oculopalatocerebral Syndrome 
Oculotrichodysplasia 
Oliver-McFarlane Syndrome  
orofaciodigital syndrome IX  
osteochondrosis +   
osteonecrosis +   
otospondylomegaepiphyseal dysplasia  
Paget's disease of bone +   
palmoplantar keratosis +   
paracoccidioidomycosis +   
Parana Hard Skin Syndrome 
Parastremmatic Dwarfism  
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 hypertrophic osteoarthropathy +   
Primary Localized Cutaneous Amyloidosis, 2  
Primary Localized Cutaneous Amyloidosis, 3  
Progressive Osseous Heteroplasia  
Progressive Vitiligo with Mental Retardation and Urethral Duplication 
Prolidase Deficiency  
Proportionate Dwarfism, with Hip Dislocation 
Pseudodiastrophic Dysplasia 
pseudoxanthoma elasticum +   
rapadilino syndrome  
Reticulate Pigmentary Disorder, with Systemic Manifestations  
Robinow syndrome +   
Rommen Mueller Sybert Syndrome 
Rothmund-Thomson syndrome +   
Ruvalcaba Syndrome 
Sclerosing Bone Dysplasia Mental Retardation 
Seckel Like Syndrome Type Buebel 
Seckel syndrome 1  
Seckel syndrome 2  
Seckel Syndrome 3 
Seckel syndrome 4  
Short Limb Dwarfism Al Gazali Type 
Short Stature and Facioauriculothoracic Malformations 
SHORT STATURE WITH MICROCEPHALY AND DISTINCTIVE FACIES  
SHORT STATURE WITH NONSPECIFIC SKELETAL ABNORMALITIES  
SHORT STATURE, DEVELOPMENTAL DELAY, AND CONGENITAL HEART DEFECTS  
SHORT STATURE, FACIAL DYSMORPHISM, AND SKELETAL ANOMALIES WITH OR WITHOUT CARDIAC ANOMALIES  
SHORT STATURE, HEARING LOSS, RETINITIS PIGMENTOSA, AND DISTINCTIVE FACIES  
Short Stature, Mental Retardation, Callosal Agenesis, Heminasal Hypoplasia, Microphthalmia, and Atypical Clefting 
SHORT STATURE, MICROCEPHALY, AND ENDOCRINE DYSFUNCTION  
SHORT STATURE, RHIZOMELIC, WITH MICROCEPHALY, MICROGNATHIA, AND DEVELOPMENTAL DELAY  
Short Stature-Obesity Syndrome 
Silver-Russell syndrome +   
Silverman-Handmaker type dyssegmental dysplasia  
Singh Chhaparwal Dhanda Syndrome 
Sjogren-Larsson syndrome +   
Skin Fragility-Woolly Hair Syndrome  
sphenoid sinusitis +  
spinal disease +   
Spondyloepiphyseal Dysplasia Tarda, Toledo Type 
Spondylometaepiphyseal Dysplasia, Short Limb-Hand Type  
Stiff Skin Syndrome  
Storm Syndrome 
Synovial Chondromatosis, Familial, with Dwarfism 
Systemic Hyalinosis  
Thoraco Limb Dysplasia Rivera Type 
Thoracomelic Dysplasia 
Tricho-Dento-Osseous Syndrome 1 
Trichothiodystrophy Syndromes +   
Trochlea of the Humerus, Aplasia of 
Tryptophanuria with Dwarfism 
visceral leishmaniasis  
Vohwinkel Syndrome, Variant Form  
Weill-Marchesani syndrome +   
Weill-Marchesani-Like Syndrome  
Whyte Murphy Syndrome 
X-linked ichthyosis +   
xeroderma pigmentosum +   
yaws +  

Synonyms
Exact Synonyms: GO ;   Geroderma Osteodysplasticum ;   Geroderma osteodysplastica ;   Geroderma osteodysplastica hereditaria ;   Walt Disney dwarfism
Primary IDs: MESH:C537799 ;   RDO:0003703
Alternate IDs: OMIM:231070

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