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LD90.Y Other specified conditions with disorders of intellectual development as a relevant clinical feature

International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01

synonyms

• Other specified conditions with disorders of intellectual development as a relevant clinical feature
• Non-syndromic conditions with disorders of intellectual development as a relevant clinical feature
• Autosomal dominant non-syndromic intellectual deficit
• Autosomal recessive non-syndromic intellectual deficit
• X-linked non-syndromic intellectual deficit
• Syndromic conditions with disorders of intellectual development as a relevant clinical feature
• ATR-X-related syndromes
• X-linked intellectual deficit - hypotonic face
• Carpenter-Waziri syndrome
• Chudley-Lowry-Hoar syndrome
• Holmes-Gang syndrome
• Juberg-Marsidi syndrome
• Renier-Gabreels-Jasper syndrome
• Smith-Fineman-Myers syndrome
• Axonal hereditary motor and sensory neuropathy, X-linked
• X-linked Charcot-Marie-Tooth disease type 2
• X-linked Charcot-Marie-Tooth disease type 3
• X-linked Charcot-Marie-Tooth disease type 4
• X-linked Charcot-Marie-Tooth disease type 5
• Cohen syndrome
• FRAXE intellectual deficit
• Hereditary hyperekplexia
• Congenital stiff man syndrome
• Hereditary hyperexplexia
• Familial Startle disease
• Stiff baby syndrome
• Hyperekplexia
• Kok disease
• Infantile bilateral striatal necrosis
• Familial infantile bilateral striatal necrosis
• Sporadic infantile bilateral striatal necrosis
• Infantile onset spinocerebellar ataxia
• Ophthalmoplegia - hypotonia - ataxia - hypoacusis - athetosis
• IOSCA - [infantile onset spinocerebellar ataxia]
• Ohaha - [Ophthalmoplegia - hypotonia - ataxia - hypoacusis - athetosis] syndrome
• L1 syndrome
• Laurence-Moon syndrome
• PEHO syndrome
• Progressive encephalopathy with oedema, hypsarrhythmia and optic atrophy
• Renpenning syndrome
• X-linked intellectual deficit, Renpenning type
• Hamel cerebro-palato-cardiac syndrome
• X-linked intellectual deficit, Fichera type
• X-linked intellectual deficit, Golabi-Ito-Hall type
• X-linked intellectual deficit, Porteous type
• X-linked intellectual deficit, Sutherland-Haan type
• X-linked intellectual deficit, Najm type
• X-linked intellectual disability, Najm type
• X-linked spastic paraplegia type 2
• Demyelinating hereditary motor and sensory neuropathy, X-linked
• X-linked Charcot-Marie-Tooth disease 1
• CMT X - [X-linked Charcot-Marie-Tooth disease 1]
• Cerebellar atrophy - ataxia - seizures
• Autosomal recessive ataxia due to ubiquinone deficiency
• Autosomal recessive ataxia due to coenzyme Q10 deficiency
• Atypical Rett syndrome
• De Sanctis-Cacchione syndrome
• SYNGAP1 syndrome
• synaptic Ras-GTPase-activating protein 1 syndrome
• Alopecia – psychomotor epilepsy – periodontal pyorrhoea – intellectual disability syndrome
• Shokeir syndrome

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