ICD-10 Lookup - Find Medical Diagnosis Codes
ICD-10 Search Results for microcephaly-q02
| ICD-10-CM Code | Description | Category | Valid for Submission |
|---|---|---|---|
| Q02 | Microcephaly Microcephaly with simplified gyral pattern; Microcephaly; Congenital microcephaly; Microcephaly, corpus callosum and cerebellar vermis hypoplasia, facial dysmorphism, intellectual disability syndrome; Early-onset progressive diffuse brain atrophy, microcephaly, muscle weakness, optic atrophy syndrome; Microcephaly, congenital cataract, psoriasiform dermatitis syndrome; Progressive microcephaly, seizures, cortical blindness, developmental delay syndrome; Postnatal microcephaly, infantile hypotonia, spastic diplegia, dysarthria, intellectual disability syndrome; X-linked microcephaly, growth retardation, prognathism, cryptorchidism syndrome; DONSON-related microcephaly, short stature, limb abnormalities spectrum; Spastic tetraplegia, thin corpus callosum, progressive postnatal microcephaly syndrome; PYCR2-related microcephaly, progressive leukoencephalopathy; Microcephaly, corpus callosum hypoplasia, intellectual disability, facial dysmorphism syndrome; Microcephaly, intellectual disability, sensorineural hearing loss, epilepsy, abnormal muscle tone syndrome; Osteogenesis imperfecta, recessive perinatal lethal, with microcephaly AND cataracts; Microcephaly, normal intelligence and immunodeficiency; Secondary microcephaly; Fetal microcephaly; Amish lethal microcephaly; Microcephaly-capillary malformation syndrome; Mandibulofacial dysostosis with microcephaly; Microcephaly with cervical spine fusion anomaly; Autosomal recessive primary microcephaly; Achalasia microcephaly syndrome; Radioulnar synostosis with microcephaly and scoliosis syndrome; Anonychia with microcephaly syndrome; Aphalangy and syndactyly with microcephaly syndrome; Severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome; Microcephaly, hypogammaglobulinemia, abnormal immunity syndrome; Agammaglobulinemia, microcephaly, craniosynostosis, severe dermatitis syndrome; Microcephaly, seizure, intellectual disability, heart disease syndrome; Epilepsy, microcephaly, skeletal dysplasia syndrome; Autosomal recessive chorioretinopathy and microcephaly syndrome; Microcephaly, thin corpus callosum, intellectual disability syndrome; Infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly; Microcephaly, short stature, intellectual disability, facial dysmorphism syndrome; X-linked colobomatous microphthalmia, microcephaly, intellectual disability, short stature syndrome; Extrasystoles, short stature, hyperpigmentation, microcephaly syndrome; Severe neonatal onset encephalopathy with microcephaly; Microcephaly, polymicrogyria, corpus callosum agenesis syndrome; Severe feeding difficulties, failure to thrive, microcephaly due to ASXL3 deficiency syndrome; Intellectual disability, feeding difficulties, developmental delay, microcephaly syndrome; THOC6-related developmental delay-microcephaly-facial dysmorphism syndrome; Porencephaly, microcephaly, bilateral congenital cataract syndrome; Hypogonadotropic hypogonadism, severe microcephaly, sensorineural hearing loss, dysmorphism syndrome; Severe intellectual disability, progressive postnatal microcephaly, midline stereotypic hand movements syndrome; Autosomal dominant primary microcephaly; Hydromicrocephaly; Diffuse cerebral and cerebellar atrophy, intractable seizures, progressive microcephaly syndrome; Primary microcephaly, mild intellectual disability, young-onset diabetes syndrome; Congenital microcephaly, severe encephalopathy, progressive cerebral atrophy syndrome; Primary microcephaly, epilepsy, permanent neonatal diabetes syndrome; | Valid |