Disease Index
9,486 diseasesDenys-Drash syndrome
Human disease
MeSH: D030321
dermal myiasis
human disease
ICD: B87.0
dermatitis herpetiformis
human disease
MeSH: D003874
Dermatitis repens
human disease
ICD: L40.2
dermatocardioskeletal syndrome boronne type
human disease
MeSH: C536577
dermatofibrosarcoma protuberans
fibrosarcoma that is located in the dermis layer of the skin
ICD: C49MeSH: D018223
Dermatoleukodystrophy
human disease
MeSH: C538220
dermatomyositis
myositis that results in inflammation located in muscle or located in skin where a skin rash is often seen prior to the onset of muscle weakness
ICD: M33.033.0-M33.133.1MeSH: D003882
Dermatoosteolysis, Kirghizian type
human disease
MeSH: C535373
dermatopathia pigmentosa reticularis
human disease
ICD: Q82.4MeSH: C535374
dermis disorder
human disease
dermis elastic tissue disorder
human disease
Dermochondrocorneal dystrophy
disease
MeSH: C535375
Dermoodontodysplasia
congenital disorder of digestive system
MeSH: C565103
Dermotrichic syndrome
human disease
DES daughter
DeSanctis–Cacchione syndrome
rare autosomal recessive inherited syndrome. It is characterized by xeroderma pigmentosum, mental retardation, dwarfism, hypogonadism, and neurologic abnormalities
MeSH: C535992
Desbuquois dysplasia
osteochondrodysplasia characterized by short stature, joint laxity, scoliosis, and advanced carpal ossification with a delta phalanx
MeSH: C535943
desmoid disease, hereditary
desmoid tumor (DT) is a benign, locally invasive soft tissue tumor associated with a high recurrence rate but with no metastatic potential
desmoplastic infantile astrocytoma/ganglioglioma
human disease
desmoplastic infantile ganglioglioma
ICD: 9412/1
desmoplastic medulloblastoma
Human disease
desmoplastic small-round-cell tumor
aggressive, rare cancer
MeSH: D058405
Desmosterolosis
Desmosterolosis is a very rare sterol biosynthesis disorder characterized by multiple congenital anomalies, failure to thrive, and intellectual disability, with elevated levels of desmosterol
MeSH: C566555
desquamative interstitial pneumonia
idiopathic interstitial pneumonia that is characterized by the accumulation of bronchiolocentric alveolar macrophages in alveolar spaces and interstitial inflammation and involves mild bronchiolar fibrosis and chronic inflammation
MeSH: C562470
deuteranopia
human disease, green color blindness
developmental anomaly of metabolic origin
human disease
developmental defect during embryogenesis
human disease
developmental delay due to methylmalonate semialdehyde dehydrogenase deficiency
human disease
MeSH: C566402
developmental delay-deafness syndrome, Hildebrand type
human disease