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Descriptor English: Congenital Bone Marrow Failure Syndromes
Descriptor Spanish: Síndromes Congénitos de Insuficiencia de la Médula Ósea
Descriptor síndromes de fracaso medular congénito
Entry term(s) SFMC
SFMH
síndrome de insuficiencia congénita de la médula ósea
síndrome hereditario de IMO
síndrome hereditario de insuficiencia de la médula ósea
síndromes de FM hereditario
síndromes de fracaso medular hereditario
Scope note: Síndromes hereditarios caracterizados por la deficiencia o la ausencia de diversas células sanguíneas debido a mutaciones que afectan al desarrollo y a la proliferación de las CÉLULAS MADRE HEMATOPOYÉTICAS.
Descriptor Portuguese: Síndrome Congênita de Insuficiência da Medula Óssea
Descriptor French: Insuffisances médullaires congénitales
Entry term(s): BMF Syndrome, Inherited
Bone Marrow Failure Syndromes, Congenital
Bone Marrow Failure Syndromes, Inherited
CBMFS
Congenital Bone Marrow Failure Syndrome
IBMFS
Inherited BMF Syndrome
Inherited BMF Syndromes
Inherited Bone Marrow Failure Syndrome
Inherited Bone Marrow Failure Syndromes
Tree number(s): C15.378.190.223.500
C16.614.183
RDF Unique Identifier: https://id.nlm.nih.gov/mesh/D000080984
Scope note: Inherited syndromes characterized by deficiency or absence of various blood cells due to mutations that affect HEMATOPOIETIC STEM CELLS development and proliferation.
Allowable Qualifiers: BL blood
CF cerebrospinal fluid
CI chemically induced
CL classification
CO complications
DG diagnostic imaging
DH diet therapy
DI diagnosis
DT drug therapy
EC economics
EH ethnology
EM embryology
EN enzymology
EP epidemiology
ET etiology
GE genetics
HI history
IM immunology
ME metabolism
MI microbiology
MO mortality
NU nursing
PA pathology
PC prevention & control
PP physiopathology
PS parasitology
PX psychology
RH rehabilitation
RT radiotherapy
SU surgery
TH therapy
UR urine
VE veterinary
VI virology
Previous Indexing: Anemia, Aplastic (1963-2019)
Bone Marrow (1964-2019)
Public MeSH Note: 2020
History Note: 2020
DeCS ID: 59062
Unique ID: D000080984
Documents indexed in the Virtual Health Library (VHL): Click here to access the VHL documents
Date Established: 2020/01/01
Date of Entry: 2019/07/08
Revision Date: 2020/05/27
Congenital Bone Marrow Failure Syndromes - Preferred
Concept UI M000649195
Scope note Inherited syndromes characterized by deficiency or absence of various blood cells due to mutations that affect HEMATOPOIETIC STEM CELLS development and proliferation.
Preferred term Congenital Bone Marrow Failure Syndromes
Entry term(s) BMF Syndrome, Inherited
Bone Marrow Failure Syndromes, Congenital
Bone Marrow Failure Syndromes, Inherited
CBMFS
Congenital Bone Marrow Failure Syndrome
IBMFS
Inherited BMF Syndrome
Inherited BMF Syndromes
Inherited Bone Marrow Failure Syndrome
Inherited Bone Marrow Failure Syndromes



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