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疾病索引

Disability, disabilities

疾病索引 · 修饰语与交叉引用

修饰语与交叉引用 · icd10cm-index-2027.xml

Disability, disabilities

heart

See: Disease, heart

Disability, disabilities

intellectual

F79

Disability, disabilities › intellectual

with

Disability, disabilities › intellectual › with

autistic features

F84.9

Disability, disabilities › intellectual › with

pathogenic CHAMP1(genetic) (variant)

F78.A9

Disability, disabilities › intellectual › with

pathogenic HNRNPH2(genetic) (variant)

F78.A9

Disability, disabilities › intellectual › with

pathogenic SATB2(genetic) (variant)

F78.A9

Disability, disabilities › intellectual › with

pathogenic SETBP1(genetic) (variant)

F78.A9

Disability, disabilities › intellectual › with

pathogenic STXBP1(genetic) (variant)

F78.A9

Disability, disabilities › intellectual › with

pathogenic SYNGAP1(genetic) (variant)

F78.A1

Disability, disabilities › intellectual

autosomal dominant

F78.A9

Disability, disabilities › intellectual

autosomal recessive

F78.A9

Disability, disabilities › intellectual

genetic related

F78.A9

Disability, disabilities › intellectual › genetic related

with

Disability, disabilities › intellectual › genetic related › with

pathogenic CHAMP1(variant)

F78.A9

Disability, disabilities › intellectual › genetic related › with

pathogenic HNRNPH2(variant)

F78.A9

Disability, disabilities › intellectual › genetic related › with

pathogenic SATB2(variant)

F78.A9

Disability, disabilities › intellectual › genetic related › with

pathogenic SETBP1(variant)

F78.A9

Disability, disabilities › intellectual › genetic related › with

pathogenic STXBP1(variant)

F78.A9

Disability, disabilities › intellectual › genetic related › with

pathogenic SYNGAP1(variant)

F78.A1

Disability, disabilities › intellectual › genetic related

specified NEC

F78.A9

Disability, disabilities › intellectual › genetic related

SYNGAP1-related

F78.A1

Disability, disabilities › intellectual

in

Disability, disabilities › intellectual › in

autosomal dominant mental retardation

F78.A9

Disability, disabilities › intellectual › in

autosomal recessive mental retardation

F78.A9

Disability, disabilities › intellectual › in

SATB2-associated syndrome

F78.A9

Disability, disabilities › intellectual › in

SETBP1 disorder

F78.A9

Disability, disabilities › intellectual › in

STXBP1 encephalopathy with epilepsy

F78.A9

See also: Encephalopathy; and see also Epilepsy

Disability, disabilities › intellectual › in

X-linked mental retardation(syndromic) (Bain type)

F78.A9

Disability, disabilities › intellectual

mild(I.Q.50-69)

F70

Disability, disabilities › intellectual

moderate(I.Q.35-49)

F71

Disability, disabilities › intellectual

profound(I.Q. under 20)

F73

Disability, disabilities › intellectual

severe(I.Q.20-34)

F72

Disability, disabilities › intellectual

specified level NEC

F78.A9

Disability, disabilities › intellectual

SYNGAP1-related

F78.A1

Disability, disabilities › intellectual

X-linked(syndromic) (Bain type)

F78.A9

Disability, disabilities

knowledge acquisition

F81.9

Disability, disabilities

learning

F81.9

Disability, disabilities

limiting activities

Z73.6

Disability, disabilities

spelling, specific

F81.81