Echinobase

Search Diseases

Alphabetic Search:

A B C D E F G H I J K L M N O P Q R S T U V W X Y Z

???pagination.result.count???

???pagination.result.page??? ???pagination.result.prev??? 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 ???pagination.result.next???

Disease	Synonyms	Description
adult mesenchymal chondrosarcoma		An adult sarcoma of soft tissue and mesenchymal ch..[+] An adult sarcoma of soft tissue and mesenchymal chondrosarcoma that is located_in the cartilage. [-]
adult mesoblastic nephroma	benign MEST; MEST; mixed epithelial and stromal tu.. [+] benign MEST; MEST; mixed epithelial and stromal tumour of kidney; [-]	A mixed neoplasm that is seen mostly in early infa..[+] A mixed neoplasm that is seen mostly in early infancy and that consists of classic and cellular (atypical) variants. [-]
adult oligodendroglioma	adult brain oligodendroglioma; grade II adult Olig.. [+] adult brain oligodendroglioma; grade II adult Oligodendroglial tumor; [-]	n_a
adult papillary meningioma		n_a
adult pineal parenchymal tumor	adult Pineal Parenchymal neoplasm;	n_a
adult pineoblastoma		n_a
adult pleomorphic rhabdomyosarcoma		n_a
adult respiratory distress syndrome	adult RDS; ARDS; Non-cardiogenic pulmonary edema; .. [+] adult RDS; ARDS; Non-cardiogenic pulmonary edema; Shock lung; [-]	A respiratory failure that results from diffuse in..[+] A respiratory failure that results from diffuse injury to the endothelium of the lung (as in sepsis, chest trauma, massive blood transfusion, aspiration of the gastric contents, or pneumonia) and is characterized by pulmonary edema with an abnormally high amount of protein in the edematous fluid and by difficult rapid breathing and hypoxemia. [-]
adult spinal cord ependymoma		n_a
adult spinal cord glioblastoma multiforme	adult Spinal Cord Glioblastoma; Glioblastoma multi.. [+] adult Spinal Cord Glioblastoma; Glioblastoma multiforme of spinal cord (disorder); [-]	n_a
adult spinal muscular atrophy	SPINAL MUSCULAR ATROPHY, ADULT FORM; SPINAL MUSCUL.. [+] SPINAL MUSCULAR ATROPHY, ADULT FORM; SPINAL MUSCULAR ATROPHY, TYPE IV; [-]	n_a
adult teratoma	adult teratoma, NOS;	n_a
adult type testicular granulosa cell tumor		n_a
adult vagina botryoid rhabdomyosarcoma		n_a
adult xanthogranuloma		n_a
adult-onset Still's disease	adult onset Still's disease; adult-onset Still dis.. [+] adult onset Still's disease; adult-onset Still disease; [-]	An arthritis that is a rare from of inflammatory a..[+] An arthritis that is a rare from of inflammatory arthritis characterized by fevers, rash, and joint pain. [-]
adult-onset autosomal dominant demyelinating leukodystrophy	ADLD; adult-onset autosomal dominant leukodystroph.. [+] ADLD; adult-onset autosomal dominant leukodystrophy; autosomal-dominant or late-onset type Pelizaeus-Merzbacher disease; [-]	A leukodystrophy characterized by onset in the 4th..[+] A leukodystrophy characterized by onset in the 4th or 5th decade of life of autonomic abnormalities, pyramidal and cerebellar dysfunction, and symmetric demyelination of the CNS that has_material_basis_in heterozygous tandem genomic duplication resulting in an extra copy of the LMNB1 gene on chromosome 5q. [-]
advanced sleep phase syndrome	familial advanced sleep-phase syndrome;	A sleep disorder that involves an altered circadia..[+] A sleep disorder that involves an altered circadian rhythm resulting in falling asleep in early evening and awaking very early in the morning. [-]
advanced sleep phase syndrome 1	familial advanced sleep phase syndrome 1; FASPS1;	An advanced sleep phase syndrome that has material..[+] An advanced sleep phase syndrome that has material basis in heterozygous mutation in the PER2 gene on chromosome 2q37. [-]
advanced sleep phase syndrome 2	familial advanced sleep phase syndrome 2; FASPS2;	An advanced sleep phase syndrome that has_material..[+] An advanced sleep phase syndrome that has_material_basis_in heterozygous mutation in the CSNK1D gene on chromosome 17q25. [-]
advanced sleep phase syndrome 3	familial advanced sleep phase syndrome 3; FASPS3;	An advanced sleep phase syndrome that has material..[+] An advanced sleep phase syndrome that has material basis in heterozygous mutation in the PER3 gene on chromosome 1p36.23. [-]
afferent loop syndrome	Afferent loop syndrome (disorder); Afferent limb s.. [+] Afferent loop syndrome (disorder); Afferent limb syndrome; [-]	A postgastrectomy syndrome that is characterized b..[+] A postgastrectomy syndrome that is characterized by obstruction of the afferent loop that arises after gastric surgery with gastrojejunostomy reconstruction. [-]
aflatoxins-related hepatocellular carcinoma		n_a
agammaglobulinemia	hypogammaglobulinemia; IGHM; mu heavy chain defici.. [+] hypogammaglobulinemia; IGHM; mu heavy chain deficiency; [-]	A B cell deficiency that is caused by a reduction ..[+] A B cell deficiency that is caused by a reduction in all types of gamma globulins. [-]
agammaglobulinemia 4	B-cell linker protein deficiency; BLNK deficiency;.. [+] B-cell linker protein deficiency; BLNK deficiency; B cell linker protein deficiency; [-]	An agammaglobulinemia that has_material_basis_in a..[+] An agammaglobulinemia that has_material_basis_in a mutation a homozygous mutation in the BLNK gene on chromosome 10q23.2. [-]
agammaglobulinemia 6		An agammaglobulinemia that has_material_basis_in h..[+] An agammaglobulinemia that has_material_basis_in homozygous mutation in the CD79B gene on chromosome 17q23. [-]
agammaglobulinemia 8B		An agammaglobulinemia that is characterized by ons..[+] An agammaglobulinemia that is characterized by onset of recurrent infections in early childhood and that has_material_basis_in homozygous loss-of-function mutation in the TCF3 gene on chromosome 19p13. [-]
agammaglobulinemia 9		An agammaglobulinemia that is characterized by rec..[+] An agammaglobulinemia that is characterized by recurrent bacterial infections associated with agammaglobulinemia and absence of circulating B cells and that has_material_basis_in homozygous or compound heterozygous mutation in the SLC39A7 gene on chromosome 6p21. [-]
age related macular degeneration	age-related macular degeneration; Senile macular d.. [+] age-related macular degeneration; Senile macular degeneration; Senile macular retinal degeneration; Age Related Maculopathies; Age Related Maculopathy; [-]	A degeneration of macula and posterior pole that i..[+] A degeneration of macula and posterior pole that is characterized by a loss of vision in the center of the visual field (the macula) resulting from damage to the retina and resulting in blurring of the sharp central vision. [-]
age related macular degeneration 1	age related maculopathy 1; ARMD1;	An age related macular degeneration associated wit..[+] An age related macular degeneration associated with polymorphism in the hemicentin gene (HMCN1) on chromosome 1q25.3-q31.1. [-]
age related macular degeneration 10	ARMD10;	An age related macular degeneration associated wit..[+] An age related macular degeneration associated with variation in the genomic region 9:112,100,000-127,500,000 (GRCh38). TLR4 has been put forth as a candidate gene. [-]
age related macular degeneration 11	ARMD11;	An age related macular degeneration conferred by v..[+] An age related macular degeneration conferred by variation in the CST3 gene on chromosome 20p11. [-]
age related macular degeneration 12	ARMD12;	An age related macular degeneration conferred by m..[+] An age related macular degeneration conferred by mutation in the CX3CR1 gene on chromosome 3p22. [-]
age related macular degeneration 13	ARMD13;	An age related macular degeneration conferred by h..[+] An age related macular degeneration conferred by heterozygous mutation in the CFI gene on chromosome 4q25. [-]
age related macular degeneration 14	ARMD14;	An age related macular degeneration associated wit..[+] An age related macular degeneration associated with variation at or near the C2 and CFB genes on chromosome 6p21. [-]
age related macular degeneration 15	ARMD15;	An age related macular degeneration conferred by v..[+] An age related macular degeneration conferred by variation in the C9 gene on chromosome 5p13. [-]
age related macular degeneration 2	ARMD2;	An age related macular degeneration conferred by v..[+] An age related macular degeneration conferred by variation in the ABCA4 gene on chromosome 1p22. [-]
age related macular degeneration 4	ARMD4;	An age related macular degeneration conferred by v..[+] An age related macular degeneration conferred by variation in the CFH gene on chromosome 1q31. [-]
age related macular degeneration 5	ARMD5;	An age related macular degeneration onferred by he..[+] An age related macular degeneration onferred by heterozygous mutation in the ERCC6 gene on chromosome 10q11. [-]
age related macular degeneration 6	ARMD6;	An age related macular degeneration conferred by h..[+] An age related macular degeneration conferred by heterozygous mutation in the RAXL1 gene on chromosome 19p13. [-]
age related macular degeneration 7	ARMD7;	An age related macular degeneration conferred by v..[+] An age related macular degeneration conferred by variation in the HTRA1 gene on chromosome 10q26. [-]
age related macular degeneration 8	ARMD8;	An age related macular degeneration that has mater..[+] An age related macular degeneration that has material basis in mutation in the ARMS2 gene, originally designated LOC387715, on chromosome 10q26 [-]
age related macular degeneration 9	ARMD9;	An age related macular degeneration conferred by v..[+] An age related macular degeneration conferred by variation in the C3 gene on chromosome 19p13. [-]
agenesis of corpus callosum, cardiac, ocular, and genital syndrome		A syndrome that is characterized by global develop..[+] A syndrome that is characterized by global developmental delay and/or intellectual disability, corpus callosum agenesis or hypoplasia, craniofacial dysmorphisms, and ocular, cardiac, and genital anomalies and that has_material_basis_in heterozygous mutation in the CDH2 gene on chromosome 18q12. [-]
agenesis of the corpus callosum with peripheral neuropathy	Andermann syndrome; Charlevoix disease; corpus cal.. [+] Andermann syndrome; Charlevoix disease; corpus callosum agenesis-neuronopathy syndrome; [-]	A neurodegenerative disease characterized by autos..[+] A neurodegenerative disease characterized by autosomal recessive inheritance with early onset of severe sensory-motor polyneuropathy, variable degree of agenesis of the corpus callosum, amyotrophy, hypotonia, and cognitive impairment that has_material_basis_in homozygous or compound heterozygous mutation in the SLC12A6 gene on chromosome 15q14. [-]
aggressive NK-cell leukemia	Aggressive NK-cell leukemia (morphologic abnormali.. [+] Aggressive NK-cell leukemia (morphologic abnormality); large granular Lymphocyte Leukemia, NK-cell type; aggressive NK-cell leukaemia; natural killer cell leukaemia; natural killer cell leukemia; [-]	A leukemia that is characterized by the systemic p..[+] A leukemia that is characterized by the systemic proliferation of NK cells closely associated with Epstein-Barr virus and that is located_in the peripheral blood, bone marrow, liver, and spleen. [-]
aggressive digital papillary adenocarcinoma		n_a
aggressive periodontitis	juvenile periodontitis;	A periodontitis that is characterized by rapid att..[+] A periodontitis that is characterized by rapid attachment loss and bone destruction in the presence of little local factors such as dental plaque and dental calculus resulting in inflammation and a loss of periodontium. [-]
aggressive systemic mastocytosis	Aggressive systemic mastocytosis (morphologic abno.. [+] Aggressive systemic mastocytosis (morphologic abnormality); ASM; Lymphadenopathic mastocytosis with eosinophilia; [-]	n_a
agnathia-otocephaly complex	agnathia-holoprosencephaly-situs inversus syndrome.. [+] agnathia-holoprosencephaly-situs inversus syndrome; dysgnathia complex agnathia-holoprosencephaly; holoprosencephaly-agnathia; otocephaly; [-]	A physical disorder characterized by mandibular hy..[+] A physical disorder characterized by mandibular hypoplasia or agnathia, ventromedial auricular malposition (melotia) and/or auricular fusion (synotia), and microstomia with oroglossal hypoplasia or aglossia. Holoprosencephaly is the most commonly identified association, but skeletal, genitourinary and cardiovascular anomalies and situs inversus have been reported. [-]

???pagination.result.page??? ???pagination.result.prev??? 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 ???pagination.result.next???