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Congenital Bone Marrow Failure Syndromes
Inherited syndromes characterized by deficiency or absence of various blood cells due to mutations that affect HEMATOPOIETIC STEM CELLS development and proliferation.
推出的年份: 2020
副标题
blood
cerebrospinal fluid
chemically induced
classification
complications
diagnosis
diagnostic imaging
diet therapy
drug therapy
economics
embryology
enzymology
epidemiology
ethnology
etiology
genetics
history
immunology
metabolism
microbiology
mortality
nursing
parasitology
pathology
physiopathology
prevention and control
psychology
radiotherapy
rehabilitation
surgery
therapy
urine
veterinary
virology
树号:
C15.378.190.223.500, C16.614.183
MeSH 单一 ID:
D000080984
进入的组:
Congenital Bone Marrow Failure Syndrome
Inherited BMF Syndrome
BMF Syndrome, Inherited
Bone Marrow Failure Syndromes, Congenital
IBMFS
CBMFS
Inherited BMF Syndromes
Bone Marrow Failure Syndromes, Inherited
Inherited Bone Marrow Failure Syndrome
Inherited Bone Marrow Failure Syndromes
早前的内容:
Anemia, Aplastic (1963-2019)
Bone Marrow (1964-2019)
All MeSH Categories
Diseases Category
Hemic and Lymphatic Diseases [C15]
Hematologic Diseases [C15.378]
Bone Marrow Diseases [C15.378.190]
Bone Marrow Failure Disorders [C15.378.190.223]
Anemia, Aplastic [C15.378.190.223.250]
Congenital Bone Marrow Failure Syndromes [C15.378.190.223.500]
Anemia, Hypoplastic, Congenital [C15.378.190.223.500.500]
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Dyskeratosis Congenita [C15.378.190.223.500.750]
Shwachman-Diamond Syndrome [C15.378.190.223.500.875]
All MeSH Categories
Diseases Category
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Infant, Newborn, Diseases [C16.614]
Amniotic Band Syndrome [C16.614.042]
Anemia, Neonatal [C16.614.053]
add_circle
Asphyxia Neonatorum [C16.614.092]
Birth Injuries [C16.614.131]
add_circle
Colic [C16.614.166]
Congenital Bone Marrow Failure Syndromes [C16.614.183]
Congenital Hyperinsulinism [C16.614.200]
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Cystic Fibrosis [C16.614.213]
Epilepsy, Benign Neonatal [C16.614.258]
Erythroblastosis, Fetal [C16.614.304]
add_circle
Hernia, Umbilical [C16.614.378]
Hydrophthalmos [C16.614.438]
Hyperbilirubinemia, Neonatal [C16.614.451]
add_circle
Hyperostosis, Cortical, Congenital [C16.614.465]
Ichthyosis [C16.614.492]
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Infant, Premature, Diseases [C16.614.521]
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Meconium Aspiration Syndrome [C16.614.580]
Mobius Syndrome [C16.614.595]
Neonatal Abstinence Syndrome [C16.614.610]
Neonatal Sepsis [C16.614.627]
Nystagmus, Congenital [C16.614.643]
Ophthalmia Neonatorum [C16.614.677]
Persistent Fetal Circulation Syndrome [C16.614.694]
Rothmund-Thomson Syndrome [C16.614.760]
Sclerema Neonatorum [C16.614.810]
Severe Combined Immunodeficiency [C16.614.815]
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Syphilis, Congenital [C16.614.868]
Thanatophoric Dysplasia [C16.614.890]
Thrombocytopenia, Neonatal Alloimmune [C16.614.899]
Toxoplasmosis, Congenital [C16.614.909]
Vitamin K Deficiency Bleeding [C16.614.940]
Wolman Disease [C16.614.947]
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