Infantile neuroaxonal dystrophy
describes several similar diseases
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Infantile neuroaxonal dystrophy
Summary
Infantile neuroaxonal dystrophy is a rare disease[1]. It has Wikipedia articles in 6 language editions, a strong signal of global cultural recognition.[2]
Key Facts
- Infantile neuroaxonal dystrophy's instance of is recorded as rare disease[3].
- Infantile neuroaxonal dystrophy's instance of is recorded as class of disease[4].
- Infantile neuroaxonal dystrophy is a type of neuroaxonal dystrophy[5].
- Infantile neuroaxonal dystrophy is a type of PLA2G6-associated neurodegeneration[6].
- Infantile neuroaxonal dystrophy comprises neurodegeneration with brain iron accumulation 2A[7].
- Infantile neuroaxonal dystrophy comprises neurodegeneration with brain iron accumulation 2B[8].
- Infantile neuroaxonal dystrophy's ICD-9-CM is recorded as 330.8[9].
- Infantile neuroaxonal dystrophy's NCI Thesaurus ID is recorded as C84927[10].
- Infantile neuroaxonal dystrophy's health specialty is recorded as neurology[11].
- Infantile neuroaxonal dystrophy's genetic association is recorded as PLA2G6[12].
- Infantile neuroaxonal dystrophy's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_2174[13].
Why It Matters
Infantile neuroaxonal dystrophy has Wikipedia articles in 6 language editions, a strong signal of global cultural recognition.[2] It is known by 8 alternative names across languages and contexts.[14]