1. No category

Common Genetic ICD-9 Codes
General Prenatal Testing
V82.4
V28.8
V28.2
V28.1
V28.0
V26.3
V26.3
796.5
795.2
659.63
659.53
(Maternal)Postnatal scrn for chrm
anomalies
CVS- Other Specified Prenatal
Test
Other screening based on
amniocentisis
Amniocentesis for Elev. AFP
Amniocentesis to r/o chromosome
abnormality
Preconceptional Genetic
Counseling
Genetic Counseling & Testing
Abnor finding on anten screening
(MSAFP screening)
non-specific Abnormal karyotype
Elderly multigravida - AMA >G2
Elderly primigravida AMA G1
Chromosomal related
279.11
655.13
655.14
758.0
758.1
758.2
758.3
758.4
758.5
758.6
758.7
758.89
Di George syndrome
Velo-cardio-facial syndrome
Fetal chromos abnormalantepartum
Fetal chromos abnormalpostpartum
Down syndrome
Trisomy 13
Trisomy 18
Autosomal deletion synd
Balanced autosomal transloc
Autosomal anomaly nec
Turner Syndrome
Klinefelter's syndrome
other condition due to
chromosome anomaly
Abnormal U/S findings:
228.1
348.0
653.63
653.64
653.7 1
653.7
653.70
655.0
655.8
655.83
655.93
655.94
656.3
656.5
656.6
656.7 1
656.7 2
656.7
656.8
658.03
658.1
740.0
740.1
741
741.00
741.01
cystic hygroma
choroid plexus cyst Cerebral
Cysts
Hydrocephal fetus-antepart
Hydrocephal fetus-postpar
Sacrococcygeal teratoma
Other fetal abn causing dispro
Other fetal disproportion-unsp
Fetal cns malformation
Fetal abnormal nec
Fetal abnormality, antepartum
complication
Fetal abnormal unspecantepartum
Fetal abnormal nos-postpartum
Fetal distress
Poor fetal growth
Excessive fetal growth
Placental Abruption
Placental Anomalies
Other placental conditions
Fetal/placental problem nec
olioghydramnios, antepartum
Premature rupture membranes
Anencephaly
Craniorachischisis
Spina bifida
Spina bifida (unspc region) with
hydro
spina bifida (cervical) with
741.02
741.03
741.9
741.90
741.91
741.92
741.93
742.0 1
742.0 2
742.0
742.1
742.2 0
742.2 1
742.2 2
742.2
742.3 1
742.3 3
742.3
742.4
746.89
749.10
749.20
749.24
756.79
756.79
756.79
761.2
789.30
789.5
793.6
761.3
746.9
hydrocephalus
spina bifida (dorsal-thoracic)
with hydrocephalus
spina bifida (lumbar) with
hydrocephalus
Meningocele
spina bifida(unspec region); no
hydrocephalus
spina bifida (cervical); no
hydrocephalus
spina bifida (dorsal-thoracic);no
hydrocephalus
spina bifida(lumbar);no
hydrocephalus
Hydroencephalocele
Exencephaly
Encephalocele
Microcephaly
Holoprosencephaly
Hemimegalencephaly
Lissencephaly
reduct. deform. of brain
Dandy Walker Malformation
hydranencephaly
Congenital hydrocephalus
Other specified anomalies of
brain
Congenital heart anomaly nec
cleft lip, unspecified
Cleft lip/palate, unspec
bilateral cleft lip and palate
Gastroschisis
Omphalocele
Oth congential anomalies of
abdomen wall
Oligohydramnios affecting
NB/FETUS
Abdon/pelvic swell, mass or
lump, unspefd site
ascites
Abnormal finding/ultrasound/
abdominal area
Polyhydramnios affect nb/fetus
unspec congenital heart
anomaly no
Pregancy Loss / fetal demise
630
656.40
674.9
631
656.43
656.4
634.90
779.9
Hydatidiform mole
intrauterine death, unspecf
Unspecified Neonatal Death
Other abnormal product of
conception
intrauterine death, antepartum
IUFD
Intrauterine death
Spontanious abortion
Stillbirth
Multiple miscarriages
646.30
Hab Abort, unspec
646.33
Habitual aborter-antepart
646.34
Habitual aborter-postpart
648.00
Diabetes in preg-unspec
648.1
Maternal diabetes
Multiple pregnancies
651.03
651.1
651.4
651.6
651.2
651.30
651.5
659.4
Twin pregnancy
Triplet pregnancy
Triplet pregnancy w/fetal loss
Other multiple preg w/fetal
loss
Quadruplet pregnancy
twin preg w fetal loss
(unspec)
Quadruplet preg w/fetal loss
Grand multiparity
Family/Genetic History
655.20
V18.4
V19.7
V19.5
V19.8
655.23
Hered.disease in fam poss.
aff.fetus
Family history, mental
retardation
Family history of
consanguinity
Family History of congenital
anomalies
Family History of other
conditions
Fetus at risk for
Herediatry/Genetic disorder
Other Reasons
655.41
655.5
655.53
655.6
656.0
656.10
656.13
656.23
658.4
659.8
663
663.0
663.1
663.2
663.4
663.6
663.8
760.71
760.71
760.8
760.9
761
761.0
761.1
762.0
762.1
762.2
762.6
762.7
764
764.90-9
susp.fetal dam.due to etoh
fetal damage d/t drug
Suspected Teratogen
exposure
Radiation fetal damage
Fetal-maternal hemorrhage
RH Immu(unspec as to ep of
care)
Rh isoimmun ante partum
condition
Other isoimmun antepartum
Infection amniotic cavity
Indicat care lab/del nec
Umbilical cord complic
Prolapse of cord
Compress cord round neck
Cord entangle with compress
nec
Short umbilical cord
Vascular lesions of cord
Umbilical cord complic nec
Maternal alcohol affect nb
Fetal Alcohol Syndrome
Maternal cond nec affect nb
Maternal cond nos affect nb
Maternal compl affect nb
Incompetent cervix affect nb
Premat rupt memb affect nb
Placenta previa affect nb
Placenta hem nec affect nb
Abnormal plac nec/nos affect
nb
Umbil cond nec affect nb
Chorioamnionitis affect nb
Slow fetal growth/malnut
Fetal Growth Retardation, nos
Postnatal
MENTAL DISORDERS
299.00
312.9
314.00
315.2
315.3
315.31
315.39
315.5
315.8
315.9
317
318.0
318.1
318.2
319
Infantile/child Autism(current)
behavior disturbance
Attention Deficit Disorder
Delayed learning
Delayed speech
Devl language disor
speech delay
Mixed development disorder
Other delays in development
Developmental delay
mild mental retardaton
Moderate mental retardation
Severe mental retardation
Profound mental retardation
Mental retardation nos
NEUROLOGIC
343.9
345.9
358.8
Infantile Cerebral Palsy
Epilepsy, unspecified
benign congenital hypotonia
EYES/VISON
743
743.0
743.06
743.10
743.30
743.45
743.61
743.63
743.69
743.9
Congenital eye anomaly
Anophthalmos
Cryptophthalmos
Microphthalmos, unspcfd
Congenital cataract nos
Aniridia
Congenital ptosis, blepharophimosis,
Spec anomaly eyelid nec
Anomaly eyelid/l/orb nec
Eye anomaly nos
EARS / HEARING
389.11
389.9
744.0
744.01
744.09
744.29
744.3
sensory hearing loss
uspecified hearing loss
Ear anomaly with impair hear
Congenital absence ext ear
Ear anomaly nec/impair hear
Ear anomaly nec
Unspec anomaly of ear NOS
CARDIAC - CEREBROVASCULAR
425.3
429.3
745.2
Cardiomyopathy, congenital
Cardiomegaly
Tetralogy of fallot
ORAL
524.04
524.06
525.8
Micrognathia
Retrognathia
disorders of teeth /jaw
ABDOMENAL
553.1
553.20
553.3
553.8
789.1
789.5
Umbilical Hernia
ventral hernia, unspcfied
Diaphragmatic hernia
Hernia, specified site
hepatomegaly
ascites
GENITAL /FERTILITY/ REPRODUCTION
256.3
Other ovarian failure
257.2
cryptorchidism
257.8
androgen insensitivity
259.0
Delay sexual development
259.1
precocious sex.dev
606.0
Azoospermia
606.1
Oligospermia
606.9
Male Infertility, unspec
608.3
Atrophy of testis
608.89
male genital disorder
626.0
amenorrhea (primary)
628.9
female infertility, unspec
629.9
Habitual aborter, not preg
646.30
Hab Abort, unspec
646.33
Habitual aborter-antepart
646.34
Habitual aborter-postpart
752.51
Undescended testes
752.61
Hypospadias
752.7
Indeterminate sex
752.9
Genital organ anomal nos
SKIN
701.1
Ichthyosis, acquired
709.09
cafe au lait
SKULL/HEAD/BRAIN
740.0
740.1
741
741.9
741.90
742.0
Anencephaly
Craniorachischisis
Spina bifida
Meningocele
spina bifida(unspec region); no hydrocephalus
Encephalocele
742.01
742.1
742.20
742.3
742.4
742.42
742.5
742.59
742.8
742.9
Hydroencephalocele
Microcephaly
Holoprosencephaly
Congenital hydrocephalus
Other specified brain anomal
Lissencephaly
oth.spec.anom. spinal cord
Spinal cord anomaly nec
Nervous system anomal
Unsp anomaly-brain,spinal cord
FACE/NECK
749.00
749.03
749.10
749.11
749.20
749.24
754.0
754.01
745.5
744.89
748.0
748.1
750.10
750.15
750.3
751.21
756.0
756.08
756.10
756.17
756.19
cleft palate unspecified
Bilat cleft palate-compl
cleft lip, unspecified
Unilat cleft lip-compl
CL/palate, unspec
Bilat cleft lip and palate
Cong skull/face/jaw def
Micrognathia
Webbing of neck
Cong anomal face & neck
Choanal atreis
Nose anomaly nec
Tongue anomaly, nos
Congenital macroglossia
Cong esoph fistula/atresia
Imperforate anus
Anomaly skull/face bone
Macrocephaly
anomalies of spine, unspecf
Spina bifida occulta
Anomaly of spine nec
HEART
745
745.0
745.1
745.2
745.4
746
746.0
746.86
746.89
747.0
747.10
747.20
747.22
747.29
747.3
747.64
747.8
747.81
747.9
Cardiac septal clos anomaly
Common truncus
Transpos of great vessel
Tetralogy of fallot
Ventricular sept defect
Other congenital heart anomaly
Pulmonary valve anomaly
Congenital heart block
Congenital heart anomaly nec
Patent ductus arteriosus
Coarctation of aorta
Cong anomaly of aorta nos
Aortic atresia/stenosis
Congl anomaly of aorta nec
Pulmonary artery anomaly
hypertrophy of lower limb
Circulatory anomaly nec
Cerebrovasc anomaly
Circulatory anomaly nos
RENAL
753
Urinary system anomaly
753.0
Renal agenesis
753.12
polycystic kidney dis, nos
753.15
Renal dysplasia
753.29
Congential hydronephrosis
753.3
Kidney anomaly nec
753.5
Bladder exstrophy
753.9
Urinary anomaly nos
LIMBS - SKELETAL
754.51
Clubbed Foot
754.51
Talipes equinovarus
754.69
Congeni valgus foot def nec
754.79
Congenital foot deform nec
754.81
Pectus excavatum
754.89
Fetal Akinesia Sequence
755
Other congen limb anomaly
755.00
Polydactyly, NOS
755.10
Syndactyly, multiple/nos
755.20
Reduc deform up limb nos
755.3
Reduct deform lower limb
755.4
Reduct deform limb nos
755.41
ectrodactyly
755.50
Upper limb anomaly nos
755.58
Congenital cleft hand
755.59
Upper limb anomaly nec
755.60
Lower limb anomaly nos
755.66
Anomaly of toes nec
755.67
Anomaly of foot nec
755.69
Lower limb anomaly nec
755.9
Congen limb anomaly nos
756.1
Macrosomia
756.0
Anomaly skull/face bone
756.08
Macrocephaly
756.10
anomalies of spine, unspecf
756.17
Spina bifida occulta
756.19
Anomaly of spine nec
756.3
756.4
756.41
756.43
756.44
756.45
756.51
756.6
756.79
756.791
756.79
757.1
757.2
757.32
757.31
757.39
757.4
757.5
Rib sternum anomaly nec
Chondrodystrophy
Achondroplasia
Chondrodysplasia Punctata
Hypochondroplasia
Thanatophoric dysplasia
Osteogenesis imperfecta
Anomaly of diaphragm
Oth cong anom of abd wall
Gastroschisis
Omphalocele
I Ichthyosis
Dermatoglyphic anomaly
Cutis Marmorata Telangiectatica Congenita
Congen ectodermal dysplas
Other spec anom of skin
Hair anomaly nec
Nail anomaly nec
CHROMOSOMES
758.0
758.1
758.2
758.3
758.4
758.5
758.6
758.7
758.81
758.89
758.9
795.2
796.5
Down syndrome /+21
Trisomy 13 / +13
Trisomy 18 / +18
Autosomal deletion synd
Balanced autosomal transloc
Autosomal anomaly nec
Turner Syndrome / -X
Klinefelter's syndrome / XXY
Other cond.due to sex chrom
other chromosome anomaly condition
Oth chromosome anomaly unspecfic
non-specific Abnormal karyotype
Abnor finding on anten screening
Congenital Anomaly / Syndromes
279.11
284.0
237.71
237.72
759.7
759.81
759.82
759.83
759.89
759.9
Di George syndrome VCF
Fanconi's Anemia
NF-1
NF-2
MCA - Multiple congenital anomaly
Prader-Willi syndrome
Marfan Syndrome
Fragile X syndrome
Congenital malformation.syn
Congenital anomaly nos
PHYSICAL GROWTH
243.0
244.9
251.2
255.2
278.00
764.90-9
765
779.82
779.9
780.39
781.0
781.2
781.3
783.1
783.22
783.4
783.4 1
783.4 2
783.40
783.41
783.42
783.43
783.9 1
784.5
786.03
congenital hypothyroidism
unspecified hypothyroidism
Hypoglycemia- unspecified
cong. adrenal hyperplasia
Obesity, unspecified
Fetal Growth Retardation, nos
Short gestat/low birthwt
cong hypotonia
Stillbirth
seizures/convulsions, NOS
Abn involuntary movements - dystonia
Ataxia (gait)
Lack of coordin-hypotonia
Abnormal Weight Gain
Underweight
Failure to thrive
short stature
Lack of Growth
lack of nml physiological dev, unspec
Failure to thrive
delayed milestones
Short Stature
Tall Stature
speech disorder, defect
Apnea
Familial / Genetic
V13.2
V13.5
V13.69
V18.4
V19.0
V19.5
V19.7
V19.8
V26.3 1
V40.0
V71.8
V71.89
V71.9
Personal Hx of genital or obsteric disorder
Personal Hx other musculoskeletal
personal Hx of other congenital
malformations
FAM Hx, mental retardation
FAM Hx Blindness
FAM Hx of congenital anomalies
FAM Hx of consanguinity
FAM Hx of other conditions
Preconceptional Genetic Counseling
Problems with learning
observ. of specif/susp cond.
Observ for other specified susp cond
observ for unspecf suspec condition
Solid Tumors & Neoplasms
200.10
155.0
171.0
171.5
171.8
171.9
173.9
183.0
186.0
186.9
188.0
188.8
188.9
190.5
198.81
198.89
198.89
199.1
200.00
202.81
202.82
202.83
202.84
202.85
202.86
202.88
203.00
203.01
223.3
233.0
233.7
236.2
236.4
236.7
239.2
239.3
Lymphosarcoma unspec
Hepatoblastoma
Malignant neoplasm of
head, face, and neck
Malignant neoplasm abdomen
Malignant neoplasm of other
specified sites of connective
and other soft tissue
Malignant neoplasm of
connective and other soft
tissue, site unspecified
Other malignant neoplasm of
skin, site unspecified
Malig neoplasm Ovary
Malig neoplasm of undes.
testis
malig neopl of oth & unspc
testis
Malignant neoplasm of trigone
of urinary bladder
Malignant neoplasm of other
specified sites of bladder
Malignant neoplasm of bladder,
Retinoblastoma
Secondary malignant
neoplasm of breast
Secondary malignant
neoplasm of other specified
sites
Neoplasm of connective tissueleg,malignant
Malig neoplasm nos,unsp site
Reticulosarcoma unspec
Other lymphomas; lymph
nodes of face, head and neck
Other lymphomas; intrathoracic
lymph nodes
Other lymphomas; intraabdominal lymph nodes
Other lymphomas; lymph
nodes of axilla and upper limb
Other lymphomas; lymph
nodes of inguinal region and
lower limb
Other lymphomas; intrapelvic
lymph nodes
Other lymphomas; lymph
nodes of multiple sites
Multiple
myeloma/immunoproliferative
neoplasms; no remission
Multiple myeloma and
immunoproliferative
neoplasms; remission
Benign neoplasm of bladder
Carcinoma in situ of breast
Carcinoma in situ of bladder
neoplasm uncertain behavior
ovary
neoplasm uncertain behavior
testis
Neoplasm of uncertain
behavior of bladder
Neoplasm of unspecified
nature of bone, soft tissue, and
skin
Neoplasm unspecified nature
239.3
239.4
of breast
neoplasms of the breast
neoplasms of the bladder
Leukemias
200.20
Burkitt's tumor unspec sites
200.21
BL (nodes of head, face,
neck)
200.28
BL mult sites
200.80
Mixed lymphosarcoma unspec
201.00
Hodgkins without remission
201.90
- disorder nos unspec
202.00
Nodular lymphoma unspec
202.10
myocosis fungoides
202.20
Sezary's disease, unspec site
202.3
Malignant histiocytosis
202.30
Malignant histiocytosis,
unspec
202.40
Hairy-cell leukem unspec
202.60
malig mast cell tumors, unsp
site
202.80
Lymphomas nec unspec site
202.9
Malignant neoplasm lym/hist
tis nec
202.90
Lymphoid mal nec unspec
203.00
Multiple Myeloma (no
remision)
203.01
Mult. myeloma (remission)
203.10
Plasma Cell leuk, (not in
remision)
203.11
Plasma cell leuk, in remi
203.8
Immunoproliferat neoplasm
nec
203.80
immunprolif neoplas, (no
remision)
204.00
ALL (not in remision)
204.01
ALL (in remision)
204.10
CLL (not in remision)
204.11
CLL (in remision)
204.2
Subac lymphoid leukemia
204.80
Other lymph leukemia (no
remision)
204.81
Other lymph leuk (in remision)
204.90
Uspec. lymph leuk(not in
remision)
204.91
unspec lymph leuk (in
remision)
205.00
AML/APL Myeloid (no
remision)
205.01
AML (in remision) APL
Myeloid
205.10
CML (not in remision)
205.11
CML (in remision)
205.2
Subacut myeloid leukemia
205.30
Myeloid sarcoma (not in
remision)
205.80
Myeloid leukemia nec (not in
remision)
205.82
Myeloid leukemia (in remision)
205.90
Myeloid leukemia nos
(noremision)
205.91
unspec myel leuk (in remision)
206.00
Acute Leukemia
206.10
Chronic monocytic leukemia
(not in remision)
206.20
Subac monocytic leukemia
(not in remision)
206.80
Monocytic leukemia nec (not
in remision)
206.90
207.00
207.10
207.20
207.80
207.81
208.0
208.00
208.01
208.10
208.2
208.80
208.81
208.9
214.0
215.0
215.4
215.9
228.00
238.4
238.6
238.7
284.8
284.9
285.0
285.22
285.9
287.1
287.5
288.0
288.9
758.89
758.9
789.1
789.2
789.30
790.09
V10.62
V10.63
V10.69
V10.71
V10.72
Monocytic leukemia nos (not
in remision)
Other specific Leukemia
Chronic erythremia (not in
remision)
Megakaryocytic leukemia (not
in remision)
other specific leukemia (not in
remision)
other specific leukemia (in
remission)
Acute leukemia nos
Acute Leukemia (not in
remision)
Acute Leukemia (in remision)
Chronic leukemia nos (not in
remision)
Subacute leukemia nos
other leukemia of unspecified
type, (not in remision)
oth leuke unspec type, in rem
Leukemia-unspec cell nos
Lipoma
benign neoplasm connective
tissue, head and neck
benign neoplasm conn tissue
and soft tissue- thorax
benign neoplasm conn tiss or
other soft tiss, unspec
Hemangioma
PCV Polycythemia vera
Myeloma (multiple)
MDS Myelodysplastic/
myeloproliferative syndrome
Acquired aplas
anem/pancytopenia
Aplastic anemia, unspec
idiopathic
sideroblastic anemia
Anemia in neoplastic disease
anemia, unspecif
thrombocytopathy
Thrombocytopenia,
unspecified
Leukopenia, neutropenia
Other specified disease of
WBCs (Leukocytosis)
other condition due to
chromosome anomaly
Oth chromosome anomly
unspecfic
Hepatomegaly
Splenomegaly
Abdon/pelvic swell, mass or
lump, unspefd site
other abnormality of red blood
cells
Myeloid leukemia
Monocyic leukemia
Other leukemia
lymphosarcoma and
reticulosarcoma
Hodgkin's disease