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Disease	Synonyms	Description	Articles
dependent personality disorder		A personality disorder that is characterized by a ..[+] A personality disorder that is characterized by a pervasive psychological dependence on other people. [-]
depersonalization disorder	Neurotic derealization;	A dissociative disorder in which the sufferer is a..[+] A dissociative disorder in which the sufferer is affected by persistent or recurrent feelings of depersonalization and/or derealization. [-]
depressive disorder	depression; mental depression;	A mood disorder characterized by persistent sadnes..[+] A mood disorder characterized by persistent sadness, emptiness, or irritability and decreased ability to function. [-]	7 articles
deprivation amblyopia	Deprivation amblyopia; disuse amblyopia;	An amblyopia that is characterized by a structural..[+] An amblyopia that is characterized by a structural anomaly that impairs vision like a droopy eyelid or an opacity in the eye, such as a cataract or corneal scar. [-]
dermal unilateral segmental cavernous angioma	Unilateral segmental cavernous hemangioma (disorde.. [+] Unilateral segmental cavernous hemangioma (disorder); Unilateral Segmental Cavernous hemangioma of the skin; Unilateral segmental cavernous hemangioma; [-]	n_a
dermatitis	skin inflammation; eczema;	A skin disease characterized by itchy, erythematou..[+] A skin disease characterized by itchy, erythematous, vesicular, weeping and crusting patches of skin. [-]	1 articles
dermatitis herpetiformis	Dermatitis herpetiformis; Dermatitis herpetiformis.. [+] Dermatitis herpetiformis; Dermatitis herpetiformis (disorder); Dermatitis herpetiformis [dup] (disorder); Duhring's disease; Dermatosis herpetiformis; [-]	n_a
dermatofibrosarcoma protuberans		A fibrosarcoma that is located_in the dermis larye..[+] A fibrosarcoma that is located_in the dermis laryer of the skin and that begins as a hard nodule and grows slowly. [-]
dermatographia	dermographism; dermatographic urticaria;	A physical urticaria induced by stroking of the sk..[+] A physical urticaria induced by stroking of the skin. [-]
dermatomycosis		A cutaneous mycosis that results in fungal infecti..[+] A cutaneous mycosis that results in fungal infection located in skin or of its appendages, has_material_basis_in Ascomycota fungi other than the dermatophytes. [-]
dermatomyositis	dermatopolymyositis; Amyopathic dermatomyositis; P.. [+] dermatopolymyositis; Amyopathic dermatomyositis; Polymyositis with skin involvement; [-]	A myositis that results_in inflammation located_in..[+] A 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. The disease may result from either a viral infection or an autoimmune reaction. [-]	1 articles
dermatopathia pigmentosa reticularis	DPR;	An ectodermal dysplasia characterized by reticulat..[+] An ectodermal dysplasia characterized by reticulate hyperpigmentation, noncicatricial alopecia, and onychodystrophy that has_material_basis_in heterozygous mutation in the KRT14 gene on chromosome 17q21.2. [-]
dermatophytosis		A cutaneous mycosis that results_in fungal infecti..[+] A cutaneous mycosis that results_in fungal infection located_in scalp, located_in glabrous skin, or located_in nail, has_material_basis_in Ascomycota fungi that belong to a group called dermatophytes, which have the ability to utilize keratin as a nutrient source. [-]
dermatosis papulosa nigra	Dermatosis papulosa nigra (disorder); Dermatosis p.. [+] Dermatosis papulosa nigra (disorder); Dermatosis papulosa nigra (morphologic abnormality); Dermatosis papulosa nigra; [-]	n_a
dermis tumor	neoplasm of Dermis; tumor of dermis; tumour of der.. [+] neoplasm of Dermis; tumor of dermis; tumour of dermis; dermis tumour; [-]	n_a
dermoid cyst	cystic dermoid choristoma; Dermoid choristoma; Mat.. [+] cystic dermoid choristoma; Dermoid choristoma; Mature cystic teratoma; teratoma, benign (morphologic abnormality); teratoma, benign; Dermoid tumour; [-]	A cystic teratoma that is composed exclusively of ..[+] A cystic teratoma that is composed exclusively of mature tissues derived from two or three germ layers (ectoderm, mesoderm and endoderm). [-]
dermoid cyst of ovary	Dermoid cyst (& [ovarian]); Dermoid cyst of ovary .. [+] Dermoid cyst (& [ovarian]); Dermoid cyst of ovary (disorder); Ovarian Dermoid Cyst; Dermoid cyst; Dermoid cyst of ovary; [-]	A dermoid cyst that is located_in the ovary.
dermoid cyst of skin	Dermoid cyst of skin (finding); skin Dermoid; Derm.. [+] Dermoid cyst of skin (finding); skin Dermoid; Dermoid cyst of skin; [-]	A dermoid cyst that is located_in the skin.
descending colon cancer	Ca descending colon (disorder); malignant neoplasm.. [+] Ca descending colon (disorder); malignant neoplasm of left colon; malignant tumor of descending colon (disorder); Ca descending colon; malignant tumor of descending colon; [-]	n_a
desmoplastic infantile ganglioglioma / desmoplastic infantile astrocytoma	Desmoplastic Infantile Astrocytoma; desmoplastic i.. [+] Desmoplastic Infantile Astrocytoma; desmoplastic infantile ganglioglioma; desmoplastic infantile ganglioglioma and desmoplastic infantile astrocytoma; [-]	A ganglioglioma occurring predominantly in the cer..[+] A ganglioglioma occurring predominantly in the cerebral hemispheres of infants, that are driven by MAPK pathway activation and composed of a mixed astrocytic and neuronal component (DIG) or an astrocytic component only (DIA) embedded in an extensive desmoplastic stroma, often containing foci of undifferentiated embryonal-like tumour cells. [-]
desmoplastic small round cell tumor	desmoplastic small round cell tumor (morphologic a.. [+] desmoplastic small round cell tumor (morphologic abnormality); desmoplastic small round-cell neoplasm; [-]	A small cell sarcoma that is characterized by a re..[+] A small cell sarcoma that is characterized by a recurrent chromosomal translocation t(11;22)(p13;q12) and the presence of small round cells in a desmoplastic stroma. It usually affects children and young adults. The most common site of involvement is the abdomen. Patients usually present with abdominal distention, pain, ascites, and a palpable abdominal mass. [-]
desmoplastic/nodular medulloblastoma	desmoplastic nodular medulloblastoma; Medulloblast.. [+] desmoplastic nodular medulloblastoma; Medulloblastoma with extensive nodularity; nodular medulloblastoma; [-]	A medulloblastoma that is characterized by the pre..[+] A medulloblastoma that is characterized by the presence of nodular, collagenous areas which do not contain reticulin, surrounded by hypercellular areas which contain an intercellular reticulin fiber network. [-]
desquamative interstitial pneumonia	RBILD; respiratory bronchiolitis-associated inters.. [+] RBILD; respiratory bronchiolitis-associated interstitial lung disease; familial desquamative interstitial pneumonitis; [-]	An idiopathic interstitial pneumonia that is chara..[+] An 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. [-]
detrusor sphincter dyssynergia		n_a
developmental and epileptic encephalopathy 100	DEE100; early infantile epileptic encephalopathy 1.. [+] DEE100; early infantile epileptic encephalopathy 100; [-]	A developmental and epileptic encephalopathy chara..[+] A developmental and epileptic encephalopathy characterized by onset of variable types of seizures in the first months or years of life preceded by global developmental delay that has_material_basis_in heterozygous mutation in the FBXO28 gene on chromosome 1q42. [-]
developmental and epileptic encephalopathy 101	DEE101; early infantile epileptic encephalopathy 1.. [+] DEE101; early infantile epileptic encephalopathy 101; [-]	A developmental and epileptic encephalopathy chara..[+] A developmental and epileptic encephalopathy characterized by early infantile epileptic encephalopathy and severe global developmental delay that has_material_basis_in homozygous mutation in the GRIN1 gene on chromosome 9q34. [-]
developmental and epileptic encephalopathy 102	DEE102; early infantile epileptic encephalopathy 1.. [+] DEE102; early infantile epileptic encephalopathy 102; [-]	A developmental and epileptic encephalopathy chara..[+] A developmental and epileptic encephalopathy characterized by global developmental delay and severe to profoundly impaired intellectual development with inability to walk or speak that has_material_basis_in homozygous or compound heterozygous mutations in the SLC38A3 gene on chromosome 3p21. [-]
developmental and epileptic encephalopathy 103	DEE103; early infantile epileptic encephalopathy 1.. [+] DEE103; early infantile epileptic encephalopathy 103; [-]	A developmental and epileptic encephalopathy chara..[+] A developmental and epileptic encephalopathy characterized by onset of various types of seizures in the first year of life that has_material_basis_in heterozygous mutation in the KCNC2 gene on chromosome 12q21. [-]
developmental and epileptic encephalopathy 104	DEE104; early infantile epileptic encephalopathy 1.. [+] DEE104; early infantile epileptic encephalopathy 104; [-]	A developmental and epileptic encephalopathy chara..[+] A developmental and epileptic encephalopathy characterized by developmental delay in the first few months of life and drug-resistant focal and generalized tonic-clonic seizures that has_material_basis_in heterozygous mutation in the ATP6V0A1 on chromosome 17q21. [-]
developmental and epileptic encephalopathy 105	DEE105; early infantile epileptic encephalopathy 1.. [+] DEE105; early infantile epileptic encephalopathy 105; [-]	A developmental and epileptic encephalopathy chara..[+] A developmental and epileptic encephalopathy characterized by onset of seizures and pituitary insufficiency in the first weeks or months of life with profoundly impaired development that has_material_basis_in homozygous or compound heterozygous mutation in the HID1 gene on chromosome 17q25. [-]
developmental and epileptic encephalopathy 106	DEE106; early infantile epileptic encephalopathy 1.. [+] DEE106; early infantile epileptic encephalopathy 106; [-]	A developmental and epileptic encephalopathy chara..[+] A developmental and epileptic encephalopathy characterized by onset of various types of frequent seizures within the first year of life and profound global developmental delay with limited ability to move and absent speech that has_material_basis_in homozygous mutation in the UFSP2 gene on chromosome 4q35. [-]
developmental and epileptic encephalopathy 107	DEE107; early infantile epileptic encephalopathy 1.. [+] DEE107; early infantile epileptic encephalopathy 107; [-]	A developmental and epileptic encephalopathy chara..[+] A developmental and epileptic encephalopathy characterized by onset of seizures in the first months of life, severe global developmental delay, profound intellectual disability, progressive microcephaly, and hypotonia that has_material_basis_in homozygous mutation in the NAPB gene on chromosome 20p11. [-]
developmental and epileptic encephalopathy 108	DEE108; early infantile epileptic encephalopathy 1.. [+] DEE108; early infantile epileptic encephalopathy 108; [-]	A developmental and epileptic encephalopathy chara..[+] A developmental and epileptic encephalopathy characterized by onset of multiple types of seizures in the first 2 years of life that has_material_basis_in heterozygous mutation in the MAST3 gene on chromosome 19p13. [-]
developmental and epileptic encephalopathy 109	DEE109;	A developmental and epileptic encephalopathy chara..[+] A developmental and epileptic encephalopathy characterized by onset of various types of seizures in the first months or years of life that has_material_basis_in heterozygous mutation in the FZR1 gene on chromosome 19p13. [-]
developmental and epileptic encephalopathy 11	DEE11; early infantile epileptic encephalopathy 11.. [+] DEE11; early infantile epileptic encephalopathy 11; [-]	A developmental and epileptic encephalopathy chara..[+] A developmental and epileptic encephalopathy characterized by infantile onset of refractory seizures, delayed neurologic development, and persistent neurologic abnormalities that has_material_basis_in heterozygous mutation in the SCN2A gene on chromosome 2q24. [-]
developmental and epileptic encephalopathy 110	DEE110; early infantile epileptic encephalopathy 1.. [+] DEE110; early infantile epileptic encephalopathy 110; [-]	A developmental and epileptic encephalopathy chara..[+] A developmental and epileptic encephalopathy characterized by profound global developmental delay and hypotonia apparent in infancy followed by onset of seizures in the first months or years of life that has_material_basis_in homozygous or compound heterozygous mutation in the CACNA2D1 gene on chromosome 7q21. [-]
developmental and epileptic encephalopathy 12	early infantile epileptic encephalopathy 12; DEE12.. [+] early infantile epileptic encephalopathy 12; DEE12; [-]	A developmental and epileptic encephalopathy chara..[+] A developmental and epileptic encephalopathy characterized by onset of refractory seizures in the first year of life with normal to mild developmental delay before onset of seizures but developmental regression and stagnation after seizure onset that has_material_basis_in homozygous or compound heterozygous mutation in the PLCB1 gene on chromosome 20p12.3. [-]
developmental and epileptic encephalopathy 14	DEE14; early infantile epileptic encephalopathy 14.. [+] DEE14; early infantile epileptic encephalopathy 14; [-]	A developmental and epileptic encephalopathy chara..[+] A developmental and epileptic encephalopathy characterized by refractory focal seizures developing by 6 months of age and arrest of psychomotor development that has_material_basis_in heterozygous mutation in the KCNT1 gene on chromosome 9q34. [-]
developmental and epileptic encephalopathy 16	DEE16; early infantile epileptic encephalopathy 16.. [+] DEE16; early infantile epileptic encephalopathy 16; [-]	A developmental and epileptic encephalopathy chara..[+] A developmental and epileptic encephalopathy characterized by seizure onset in the first weeks or months of life, delayed or regression of psychomotor development, and hypotonia that has_material_basis_in homozygous or compound heterozygous mutation in the TBC1D24 gene on chromosome 16p13. [-]
developmental and epileptic encephalopathy 17	DEE17; early infantile epileptic encephalopathy 17.. [+] DEE17; early infantile epileptic encephalopathy 17; [-]	A developmental and epileptic encephalopathy chara..[+] A developmental and epileptic encephalopathy characterized by onset in the first weeks or months of life of intractable seizures and very poor psychomotor development that has_material_basis_in heterozygous mutation in the GNAO1 gene on chromosome 16q13. [-]
developmental and epileptic encephalopathy 18	DEE18; early infantile epileptic encephalopathy 18.. [+] DEE18; early infantile epileptic encephalopathy 18; [-]	A developmental and epileptic encephalopathy chara..[+] A developmental and epileptic encephalopathy characterized by absence of developmental milestones, dysmorphic facial features, refractory seizures, and thick corpus callosum and persistent cavum septum pellucidum on brain imaging and that has_material_basis_in homozygous or compound heterozygous mutation in the SZT2 gene on chromosome 1p34. [-]
developmental and epileptic encephalopathy 2	DEE2; EIEE2; X-linked infantile spasm syndrome 2; .. [+] DEE2; EIEE2; X-linked infantile spasm syndrome 2; early infantile epileptic encephalopathy 2; [-]	A developmental and epileptic encephalopathy chara..[+] A developmental and epileptic encephalopathy characterized by X-linked dominant inheritance of seizure onset in the first months of life, intellectual disability, and poor motor control that has_material_basis_in mutation in the CDKL5 gene on chromosome Xp22. [-]
developmental and epileptic encephalopathy 21	DEE21; early infantile epileptic encephalopathy 21.. [+] DEE21; early infantile epileptic encephalopathy 21; [-]	A developmental and epileptic encephalopathy chara..[+] A developmental and epileptic encephalopathy characterized by onset in the first months of life by intractable seizures and severely impaired psychomotor development that has_material_basis_in homozygous or compound heterozygous mutation in the NECAP1 gene on chromosome 12p13. [-]
developmental and epileptic encephalopathy 23	DEE23; early infantile epileptic encephalopathy 23.. [+] DEE23; early infantile epileptic encephalopathy 23; Early-onset epileptic encephalopathy-cortical blindness-intellectual disability-facial dysmorphism syndrome; Epilepsy-cortical blindness-intellectual disability-facial dysmorphism syndrome; [-]	A developmental and epileptic encephalopathy chara..[+] A developmental and epileptic encephalopathy characterized by onset in the first months of life of intractable seizures, severely impaired psychomotor development with poor or absent speech, cortical blindness, and dysmorphic facial features that has_material_basis_in homozygous or compound heterozygous mutation in the DOCK7 gene on chromosome 1p31. [-]
developmental and epileptic encephalopathy 25	developmental and epileptic encephalopathy 25, wit.. [+] developmental and epileptic encephalopathy 25, with amelogenesis imperfecta; early infantile epileptic encephalopathy 25; DEE25; [-]	A developmental and epileptic encephalopathy chara..[+] A developmental and epileptic encephalopathy characterized by onset in early infancy of refractory seizures, global developmental delay with intellectual disability, persistent neurologic symptoms, and dental anomalies that has_material_basis_in homozygous or compound heterozygous mutation in the SLC13A5 gene on chromosome 17p13. [-]
developmental and epileptic encephalopathy 26	DEE26; early infantile epileptic encephalopathy 26.. [+] DEE26; early infantile epileptic encephalopathy 26; [-]	A developmental and epileptic encephalopathy chara..[+] A developmental and epileptic encephalopathy characterized by onset in the first years of life of seizures, developmental delay, intellectual disability, poor speech, and behavioral abnormalities that has_material_basis_in heterozygous mutation in the KCNB1 gene on chromosome 20q13. [-]
developmental and epileptic encephalopathy 27	DEE27; early infantile epileptic encephalopathy 27.. [+] DEE27; early infantile epileptic encephalopathy 27; [-]	A developmental and epileptic encephalopathy chara..[+] A developmental and epileptic encephalopathy characterized by early onset seizures, delayed psychomotor development and intellectual disability with variable severity that has_material_basis_in heterozygous mutation in the GRIN2B gene on chromosome 12p12. [-]
developmental and epileptic encephalopathy 31A	DEE31; early infantile epileptic encephalopathy 31.. [+] DEE31; early infantile epileptic encephalopathy 31; DEE31A; developmental and epileptic encephalopathy 31; [-]	A developmental and epileptic encephalopathy chara..[+] A developmental and epileptic encephalopathy characterized by onset in the first months or years of life of refractory seizures and global developmental delay from early infancy that has_material_basis_in heterozygous mutation in the DNM1 gene on chromosome 9q34. [-]
developmental and epileptic encephalopathy 31B	DEE31B;	A developmental and epileptic encephalopathy chara..[+] A developmental and epileptic encephalopathy characterized by early-onset epilepsy, generalized muscular hypotonia, visual impairment, and severe neurodevelopmental delay that has_material_basis_in homozygous mutation in the DNM1 gene on chromosome 9q34. [-]
developmental and epileptic encephalopathy 32	DEE32; early infantile epileptic encephalopathy 32.. [+] DEE32; early infantile epileptic encephalopathy 32; [-]	A developmental and epileptic encephalopathy chara..[+] A developmental and epileptic encephalopathy characterized by seizure onset between 5 and 17 months of age resulting in residual neurologic deficits; in some patients seizures may remit or respond to drug treatment, and that has_material_basis_in heterozygous mutation in the KCNA2 gene on chromosome 1p13. [-]

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