Pages that link to "Property:P89"
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The following pages link to Linked ICD 10 (P89):
Displaying 50 items.
- Chemical meningitis (Q41003) (← links)
- Infectious meningitis, not elsewhere classified (Q41004) (← links)
- Parasitic or protozoal meningitis (Q41005) (← links)
- Fungal myelitis (Q41006) (← links)
- Infectious encephalitis, not elsewhere classified (Q41007) (← links)
- Myelitis (Q41008) (← links)
- Parasitic myelitis (Q41009) (← links)
- Parasitic or protozoal encephalitis (Q41010) (← links)
- Infectious myelitis, not elsewhere classified (Q41011) (← links)
- Fungal encephalitis (Q41012) (← links)
- Human T-cell lymphotropic virus-associated myelopathy (Q41013) (← links)
- Bacterial encephalitis (Q41014) (← links)
- Bacterial myelitis (Q41015) (← links)
- Multiple or widespread intracranial abscess (Q41016) (← links)
- Abscess of the corpus callosum (Q41017) (← links)
- Intracranial abscess (Q41018) (← links)
- Fungal intracranial granuloma (Q41019) (← links)
- Intracranial granuloma (Q41020) (← links)
- Pituitary abscess (Q41021) (← links)
- Deep cerebral hemispheric abscess (Q41022) (← links)
- Huntington disease (Q41023) (← links)
- Ataxia due to abetalipoproteinemia (Q41024) (← links)
- Ataxia due to alcoholic cerebellar degeneration (Q41025) (← links)
- Hereditary ataxia (Q41026) (← links)
- Acquired ataxia (Q41027) (← links)
- Late onset cerebellar cortical atrophy (Q41028) (← links)
- Spinocerebellar ataxia (Q41029) (← links)
- Non-hereditary degenerative ataxia (Q41030) (← links)
- Friedreich ataxia (Q41031) (← links)
- Hereditary episodic ataxia (Q41032) (← links)
- Ataxia due to Cerebrotendinous xanthomatosis (Q41033) (← links)
- Ataxia due to mitochondrial mutations (Q41034) (← links)
- Ataxic disorders (Q41035) (← links)
- Ataxia due to Refsum disease (Q41036) (← links)
- Congenital ataxia (Q41037) (← links)
- Hereditary spastic paraplegia (Q41038) (← links)
- X-linked hereditary spastic paraplegia (Q41039) (← links)
- Autosomal recessive hereditary spastic paraplegia (Q41040) (← links)
- Autosomal dominant hereditary spastic paraplegia (Q41041) (← links)
- Late infantile spinal muscular atrophy, Type II (Q41042) (← links)
- Localised spinal muscular atrophy (Q41043) (← links)
- Adult onset spinal muscular atrophy, Type IV (Q41044) (← links)
- Juvenile form spinal muscular dystrophy, Type III (Q41045) (← links)
- Spinal muscular atrophy (Q41046) (← links)
- Infantile spinal muscular atrophy, Type I (Q41047) (← links)
- Progressive bulbar palsy (Q41048) (← links)
- Primary lateral sclerosis (Q41049) (← links)
- Monomelic amyotrophy (Q41050) (← links)
- Progressive muscular atrophy (Q41051) (← links)
- Motor neuron disease (Q41052) (← links)
