Free ICD-9-CM Diagnosis Codes Lookup
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2008
> Diseases Of The Blood And Blood-Forming Organs
280-289
> Acquired hemolytic anemias
283.*
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2008 ICD-9-CM Diagnosis Code 283.9
Acquired hemolytic anemia unspecified
283.2
284
283.9 is a billable ICD-9-CM medical code that can be used to specify a diagnosis on a reimbursement claim.
Newer versions of 283.9:
2009
2010
Also applicable to/known as
Acquired hemolytic anemia NOS
Chronic idiopathic hemolytic anemia
ICD-9-CM Volume 2 Index Entries That Refer To 283.9
Abrami's disease (acquired hemolytic jaundice)
283.9
Acholuric jaundice (familial) (splenomegalic) (see also Spherocytosis)
282.0
acquired
283.9
Anemia
285.9
Dyke-Young type (secondary)
(symptomatic)
283.9
hemolytic
283.9
acquired
283.9
with hemoglobinuria NEC
283.2
autoimmune (cold type) (idiopathic) (primary) (secondary) (symptomatic) (warm type)
283.0
due to
cold reactive antibodies
283.0
drug exposure
283.0
warm reactive antibodies
283.0
fragmentation
283.19
idiopathic (chronic)
283.9
infectious
283.19
autoimmune
283.0
non-autoimmune
283.10
toxic
283.19
traumatic cardiac
283.19
acute
283.9
due to enzyme deficiency NEC
282.3
fetus or newborn (see also Disease, hemolytic)
773.2
late
773.5
Lederer's (acquired infectious hemolytic anemia)
283.19
autoimmune (acquired)
283.0
chronic
282.9
idiopathic
283.9
cold type (secondary) (symptomatic)
283.0
congenital (spherocytic) (see also Spherocytosis)
282.0
nonspherocytic - see Anemia, hemolytic, nonspherocytic, congenital
drug-induced
283.0
enzyme deficiency
282.2
due to
cardiac conditions
283.19
drugs
283.0
enzyme deficiency NEC
282.3
drug-induced
282.2
presence of shunt or other internal prosthetic device
283.19
thrombotic thrombocytopenic purpura
446.6
elliptocytotic (see also Elliptocytosis)
282.1
familial
282.9
hereditary
282.9
due to enzyme deficiency NEC
282.3
specified NEC
282.8
idiopathic (chronic)
283.9
infectious (acquired)
283.19
mechanical
283.19
microangiopathic
283.19
nonautoimmune
283.10
nonspherocytic
congenital or hereditary NEC
282.3
glucose-6-phosphate dehydrogenase deficiency
282.2
pyruvate kinase (PK) deficiency
282.3
type I
282.2
type II
282.3
type I
282.2
type II
282.3
of or complicating pregnancy
648.2
resulting from presence of shunt or other internal prosthetic device
283.19
secondary
283.19
autoimmune
283.0
sickle-cell - see Disease, sickle-cell
Stransky-Regala type (Hb-E) (see also Disease, hemoglobin)
282.7
symptomatic
283.19
autoimmune
283.0
acute
285.1
toxic (acquired)
283.19
uremic (adult) (child)
283.11
warm type (secondary) (symptomatic)
283.0
idiopathic
285.9
hemolytic, chronic
283.9
Disease, diseased - see also Syndrome
Abrami's (acquired hemolytic jaundice)
283.9
Widal-Abrami (acquired hemolytic jaundice)
283.9
Dyke-Young anemia or syndrome (acquired macrocytic hemolytic anemia) (secondary) (symptomatic)
283.9
Hayem-Widal syndrome (acquired hemolytic jaundice)
283.9
Icteroanemia, hemolytic (acquired)
283.9
congenital (see also Spherocytosis)
282.0
Icterus (see also Jaundice)
782.4
hematogenous (acquired)
283.9
hemolytic (acquired)
283.9
congenital (see also Spherocytosis)
282.0
Jaundice (yellow)
782.4
acholuric (familial) (splenomegalic) (see also Spherocytosis)
282.0
acquired
283.9
hematogenous
283.9
hemolytic (acquired)
283.9
congenital (see also Spherocytosis)
282.0
Syndrome - see also Disease
Dyke-Young (acquired macrocytic hemolytic anemia)
283.9
Hayem-Widal (acquired hemolytic jaundice)
283.9
Widal (-Abrami) (acquired hemolytic jaundice)
283.9
Widal (-Abrami) syndrome (acquired hemolytic jaundice)
283.9