Approved Diagnostic Codes for Persons with Related …

Approved Diagnostic Codes for Persons with Related

Conditions

Effective October 1, 2023 to September 30, 2024

The following diagnostic codes are found in the International Classification of

Diseases, Tenth Revision, Clinical Modification (ICD-10-CM), 2024, and are

recognized by the Health and Human Services Commission (HHSC) as conditions

which might qualify an individual as having a related condition as described in

federal and state law.

In accordance with the Code of Federal Regulations, Title 42, 435.1010, a related

condition is a severe and chronic disability that:

A. is attributed to:

i

cerebral palsy or epilepsy; or

ii

any other condition, other than mental illness, found to be closely related

to intellectual disability because the condition results in impairment of

general intellectual functioning or adaptive behavior similar to that of

individuals with intellectual disability, and requires treatment or services

similar to those required for individuals with intellectual disability;

B. is manifested before the individual reaches age 22;

C. is likely to continue indefinitely; and

D. results in substantial functional limitation in at least three of the following

areas of major life activity:

i

self-care;

ii

understanding and use of language;

iii learning;

iv mobility;

v

self-direction; and

vi capacity for independent living.

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Texas Health and Human Services ¡ñ hhs. ¡ñ Revised: 10/2023

A primary diagnosis by a licensed physician (or designee as defined in program

rules) of a related condition may be required to meet eligibility for the following

Medicaid programs:

¡ñ

Intermediate Care Facilities for Individuals with an Intellectual Disability or

Related Conditions (ICF/IID);

¡ñ

Community Living Assistance and Support Services (CLASS);

¡ñ

Home and Community-based Services (HCS);

¡ñ

Texas Home Living (TxHmL); and

¡ñ

Deaf Blind with Multiple Disabilities (DBMD).

Please refer to the applicable rules governing those programs for complete

information regarding eligibility.

Disclaimer: the ICD-10 codes contained in the following list are subject to change

at least once a year on October 1, but can also change during the year.

Approved Diagnostic Codes for Persons with Related Conditions

Effective October 1, 2023 to September 30, 2024

ICD-10 CM - Diagnosis

Code

B91

C71.1

C71.2

C71.3

C71.4

C71.5

C71.6

C71.7

C71.8

C71.9

C79.31

C96.0

C96.5

C96.6

D42.0

D42.1

D42.9

ICD-10 CM - Diagnosis Description

Sequelae of poliomyelitis

Malignant neoplasm of frontal lobe

Malignant neoplasm of temporal lobe

Malignant neoplasm of parietal lobe

Malignant neoplasm of occipital lobe

Malignant neoplasm of cerebral ventricle

Malignant neoplasm of cerebellum

Malignant neoplasm of brain stem

Malignant neoplasm of overlapping sites of brain

Malignant neoplasm of brain, unspecified

Secondary malignant neoplasm of brain

Multifocal and multisystemic (disseminated)

Langerhans-cell histiocytosis

Multifocal and unisystemic Langerhans-cell

histiocytosis

Unifocal Langerhans-cell histiocytosis

Neoplasm of uncertain behavior of cerebral meninges

Neoplasm of uncertain behavior of spinal meninges

Neoplasm of uncertain behavior of meninges,

unspecified

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Texas Health and Human Services ¡ñ hhs. ¡ñ Revised: 10/2023

ICD-10 CM - Diagnosis

Code

D43.0

D43.1

D43.2

D43.4

D44.0

D44.10

D44.11

D44.12

D44.2

D44.3

D44.4

D44.5

D44.6

D44.7

D44.9

D49.6

D69.42

D69.49

D82.1

E00.0

E00.1

E00.2

E00.9

E03.0

E03.1

E03.2

E03.3

E03.9

E20.1

E21.0

E21.1

E21.2

E21.3

E72.03

E72.81

E72.89

E75.00

E75.02

E75.09

ICD-10 CM - Diagnosis Description

Neoplasm of uncertain behavior of brain,

supratentorial

Neoplasm of uncertain behavior of brain,

infratentorial

Neoplasm of uncertain behavior of brain, unspecified

Neoplasm of uncertain behavior of spinal cord

Neoplasm of uncertain behavior of thyroid gland

Neoplasm of uncertain behavior of unspecified

adrenal gland

Neoplasm of uncertain behavior of right adrenal gland

Neoplasm of uncertain behavior of left adrenal gland

Neoplasm of uncertain behavior of parathyroid gland

Neoplasm of uncertain behavior of pituitary gland

Neoplasm of uncertain behavior of craniopharyngeal

duct

Neoplasm of uncertain behavior of pineal gland

Neoplasm of uncertain behavior of carotid body

Neoplasm of uncertain behavior of aortic body and

other paraganglia

Neoplasm of uncertain behavior of unspecified

endocrine gland

Neoplasm of unspecified behavior of brain

Congenital and hereditary thrombocytopenia purpura

Other primary thrombocytopenia

Di Georges syndrome

Congenital iodine-deficiency syndrome, neurological

type

Congenital iodine-deficiency syndrome,

myxedematous type

Congenital iodine-deficiency syndrome, mixed type

Congenital iodine-deficiency syndrome, unspecified

Congenital hypothyroidism with diffuse goiter

Congenital hypothyroidism without goiter

Hypothyroidism due to medicaments and other

exogenous substances

Postinfectious hypothyroidism

Hypothyroidism, unspecified

Pseudohypoparathyroidism

Primary hyperparathyroidism

Secondary hyperparathyroidism, not elsewhere

classified

Other hyperparathyroidism

Hyperparathyroidism, unspecified

Lowes syndrome

Disorders of gamma aminobutyric acid metabolism

Other specified disorders of amino-acid metabolism

GM2 gangliosidosis, unspecified

Tay-Sachs disease

Other GM2 gangliosidosis

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Texas Health and Human Services ¡ñ hhs. ¡ñ Revised: 10/2023

ICD-10 CM - Diagnosis

Code

E75.19

E75.21

E75.22

E75.23

E75.240

E75.241

E75.242

E75.243

E75.244

E75.248

E75.249

E75.25

E75.29

E75.4

E76.01

E76.02

E76.03

E76.1

E76.210

E76.211

E76.219

E76.22

E79.1

E79.2

E79.81

E79.82

E79.89

E83.59

E88.9

E89.0

F07.0

F07.81

F09

F84.0

F84.2

F84.3

F84.5

F84.8

F84.9

F95.2

G00.9

G04.90

G04.91

G05.3

G05.4

ICD-10 CM - Diagnosis Description

Other gangliosidosis

Fabry (-Anderson) disease

Gaucher disease

Krabbe disease

Niemann-Pick disease type A

Niemann-Pick disease type B

Niemann-Pick disease type C

Niemann-Pick disease type D

Niemann-Pick disease type A/B

Other Niemann-Pick disease

Niemann-Pick disease, unspecified

Metachromatic leukodystrophy

Other sphingolipidosis

Neuronal ceroid lipofuscinosis

Hurlers syndrome

Hurler-Scheie syndrome

Scheies syndrome

Mucopolysaccharidosis, type II

Morquio A mucopolysaccharidoses

Morquio B mucopolysaccharidoses

Morquio mucopolysaccharidoses, unspecified

Sanfilippo mucopolysaccharidoses

Lesch-Nyhan syndrome

Myoadenylate deaminase deficiency

Aicardi-Goutieres Syndrome

Hereditary Xanthinuria

Oth Disrd Of Purine and Pyrimidine Metabolism

Other disorders of calcium metabolism

Metabolic disorder, unspecified

Postprocedural hypothyroidism

Personality change due to known physiological

condition

Postconcussional syndrome

Unspecified mental disorder due to known

physiological condition

Autistic disorder

Retts syndrome

Other childhood disintegrative disorder

Aspergers Syndrome

Other pervasive developmental disorders

Pervasive developmental disorder, unspecified

Tourettes disorder

Bacterial meningitis, unspecified

Encephalitis and encephalomyelitis, unspecified

Myelitis, unspecified

Encephalitis and encephalomyelitis in diseases

classified elsewhere

Myelitis in diseases classified elsewhere

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Texas Health and Human Services ¡ñ hhs. ¡ñ Revised: 10/2023

ICD-10 CM - Diagnosis

Code

G10

G11.10

G11.11

G11.19

G11.3

G11.4

G12.1

G12.9

G14

G20.A1

G20.A2

G20.B1

G20.B2

G20.C

G21.11

G21.19

G21.2

G21.3

G21.4

G21.8

G21.9

G23.0

G23.1

G23.2

G24.1

G31.01

G31.81

G31.82

G31.89

G35

G37.9

G40.101

G40.109

G40.111

G40.119

ICD-10 CM - Diagnosis Description

Huntingtons disease

Early-onset cerebellar ataxia, unspecified

Friedreich ataxia

Other early-onset cerebellar ataxia

Cerebellar ataxia with defective DNA repair

Hereditary Spastic Paraparesis/Paraplegia

Other inherited spinal muscular atrophy

Spinal muscular atrophy, unspecified

Postpolio syndrome

Parkinson's dis w/o dyskinesia, w/o mention of

fluctuations

Parkinson's disease without dyskinesia, with

fluctuations

Parkinson's dis with dyskinesia, w/o mention of

fluctuations

Parkinson's disease with dyskinesia, with fluctuations

Parkinsonism, unspecified

Neuroleptic induced parkinsonism

Other drug induced secondary parkinsonism

Secondary parkinsonism due to other external agents

Postencephalitic parkinsonism

Vascular parkinsonism

Other secondary parkinsonism

Secondary parkinsonism, unspecified

Hallervorden-Spatz disease

Progressive supranuclear ophthalmoplegia [SteeleRichardson- Olszewski]

Striatonigral degeneration

Genetic torsion dystonia

Picks disease

Alpers disease

Leighs disease

Other specified degenerative diseases of nervous

system

Multiple sclerosis

Demyelinating disease of central nervous system,

unspecified

Localization-related (focal) (partial) symptomatic

epilepsy and epileptic syndromes with simple partial

seizures, not intractable, with status epilepticus

Localization-related (focal) (partial) symptomatic

epilepsy and epileptic syndromes with simple partial

seizures, not intractable, without status epilepticus

Localization-related (focal) (partial) symptomatic

epilepsy and epileptic syndromes with simple partial

seizures, intractable, with status epilepticus

Localization-related (focal) (partial) symptomatic

epilepsy and epileptic syndromes with simple partial

seizures, intractable, without status epilepticus

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Texas Health and Human Services ¡ñ hhs. ¡ñ Revised: 10/2023

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