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About:
clgo:
Rare_disease
Property
Value
rdf:
type
owl:
Class
rdfs:
label
Rare disease
rdfs:
subClassOf
Human disease or disorder
prov:
wasDerivedFrom
http://en.wikipedia.org/wiki/Category:Rare_diseases
is
rdf:
type
of
Acromesomelic dysplasia
Extraskeletal Ewing sarcoma
Hemiplegic migraine
Letterer–Siwe disease
Oculopharyngeal muscular dystrophy
Catamenial pneumothorax
EAST syndrome
Familial isolated vitamin E deficiency
Mismatch repair cancer syndrome
Nodding disease
Parry–Romberg syndrome
TNF receptor associated periodic syndrome
AIDS dysmorphic syndrome
Beta thalassemia
Conjoined twins
Corticobasal degeneration
Köhler disease
Maple syrup urine disease
Townes–Brocks syndrome
Lhermitte–Duclos disease
Fukuyama congenital muscular dystrophy
Metachondromatosis
Tracheobronchomalacia
Uhl anomaly
Argininosuccinic aciduria
Asplenia with cardiovascular anomalies
Cytochrome P450 oxidoreductase deficiency
Glycogen storage disease type VI
Ichthyosis hystrix
Keratolytic winter erythema
Prolidase deficiency
Snijders Blok-Campeau syndrome
Thyroid hormone resistance
Urocanic aciduria
Urticaria pigmentosa
Zadik–Barak–Levin syndrome
Batten disease
Danon disease
Finnish heritage disease
Infantile Refsum disease
Leukocyte adhesion deficiency
Familial hemiplegic migraine
Hemihydranencephaly
ICD coding for rare diseases
Center of expertise for rare diseases
Hypertrichosis
Mulibrey nanism
CHIME syndrome
Degos disease
Familial nasal acilia
Leukodystrophy
Microcephalic primordial dwarfism, Montreal type
Autosomal recessive polycystic kidney disease
Citrullinemia type I
Glucose-galactose malabsorption
Hyperkalemic periodic paralysis
Lysosomal acid lipase deficiency
Persistent truncus arteriosus
Short-limb skeletal dysplasia with severe combined immunodeficiency
Birdshot chorioretinopathy
Fabry disease
Gastric atresia
Lymphangioleiomyomatosis
Pulmonary alveolar proteinosis
X-linked lymphoproliferative disease
Albright's hereditary osteodystrophy
Florid cutaneous papillomatosis
Fumarase deficiency
Transient acantholytic dermatosis
Weaver syndrome
Cerebroretinal microangiopathy with calcifications and cysts
Ichthyosis vulgaris
Papillary fibroelastoma
Ring chromosome 15
Scott syndrome
Wieacker syndrome
Cenani–Lenz syndactylism
Severe combined immunodeficiency
Guanidinoacetate methyltransferase deficiency
Jones syndrome
Leontiasis ossea
Megacystis (fetal)
Pycnodysostosis
Thai symphalangism syndrome
Infantile neuroaxonal dystrophy
Macrophagic myofasciitis
Congenital disorder of glycosylation type IIc
Epidermodysplasia verruciformis
Hartnup disease
Paroxysmal extreme pain disorder
Rabbit syndrome
Calpainopathy
Endocardial fibroelastosis
Isolated 17,20-lyase deficiency
Juvenile osteoporosis
Lymphomatoid papulosis
Osteochondrodysplasia
Yunis–Varon syndrome
Iridogoniodysgenesis, dominant type
Kienböck's disease
... and more
is
rdfs:
subClassOf
of
Rare infectious disease
Motor neuron disease
Rare cancer
Mitochondrial disease