Heterogeneity of GATA2-related myeloid neoplasms

Alveolarna proteinoza

Alveolarna proteinoza je difiizno oboljenje pluća koje karakteriše akumulacija u alveolama, gustog granuliranog sadržaja bogatog proteinima i lipidima, bez promena u…

ابيضاض الدم الوحيدي النقوي المزمن

ابيضاض الدم الوحيدي النقوي المزمن (CMML) هو أحد أنواع ابيضاضات الدم، وهي سرطانات تصيب الخلايا المكونة للدم في نخاع العظام.

Síndrome MonoMAC

GATA2

GATA2 o factor de unión a GATA 2 es un factor de transcripción , es decir, una proteína nuclear que regula la expresión de genes . Regula muchos genes que son críticos…

ورم لنفاوی

نقص العدلات الخلقي الشديد

急性骨髓性白血病

صمم حسي عصبي

अक्यूट मयलेईोड डिसीज़

GATA2

GATA2 is a human gene which makes a protein called GATA binding protein 2 - a transcription factor.

MonoMAC

MonoMAC ((also termed MonoMAC/DCML or Monocytopenia and Mycobacterium Avium Complex/Dendritic Cell, Monocyte, B and NK Lymphocyte deficiency) is a rare autosomal…

Chronic myelomonocytic leukemia

Chronic myelomonocytic leukaemia (CMML) is a type of leukaemia, which are cancers of the blood-forming cells of the bone marrow.

Kostmann syndrome

Kostmann syndrome is a group of diseases that affect myelopoiesis, causing a congenital form of neutropenia, usually without other physical malformations.

Lymphedema

Lymphedema, also known as lymphoedema and lymphatic edema, is a condition of localized swelling caused by a compromised lymphatic system.

Sensorineural hearing loss

Sensorineural hearing loss (SNHL) is a type of hearing loss, or deafness, in which the root cause lies in the inner ear or sensory organ (cochlea and associated…

Myelodysplastic syndrome

Myelodysplastic syndromes (MDS) are a group of cancers in which immature blood cells in the bone marrow do not mature and therefore do not become healthy blood cells.

GATA2 deficiency

GATA2 deficiency (also termed GATA2 haploinsufficiency or GATA2 deficiency syndrome) is a recently defined grouping of several disorders caused by common defect, viz.…

Pulmonary alveolar proteinosis

Pulmonary alveolar proteinosis (PAP) is a group of rare lung disorders characterized by abnormal accumulation of surfactant-derived lipoprotein compounds within the…

Emberger syndrome

The Emberger syndrome is a rare, autosomal dominant, genetic disorder caused by familial or sporadic inactivating mutations in one of the two parental GATA2 genes.