Majeed syndrome
Majeed syndrome is a rare genetic multisystemic disorder characterized by the triad of chronic recurrent multifocal osteomyelitis, congenital dyserythropoietic anemia, and variable transient inflammatory dermatosis
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Majeed syndrome
Summary
Majeed syndrome is a hereditary disorder[1]. It has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[2]
Key Facts
- Majeed syndrome's instance of is recorded as hereditary disorder[3].
- Majeed syndrome's instance of is recorded as class of disease[4].
- Majeed syndrome is a type of autoinflammatory syndrome with skin involvement[5].
- Majeed syndrome is a type of autoinflammatory syndrome with immune deficiency[6].
- Majeed syndrome is a type of constitutional dyserythropoietic anemia[7].
- Majeed syndrome is a type of pyogenic autoinflammatory syndrome[8].
- Majeed syndrome's ICD-9-CM is recorded as 759.89[9].
- Majeed syndrome's NCI Thesaurus ID is recorded as C119058[10].
- Majeed syndrome's health specialty is recorded as medical genetics[11].
- Majeed syndrome's genetic association is recorded as LPIN2[12].
- Majeed syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_77297[13].
Why It Matters
Majeed syndrome has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[2] It is known by 7 alternative names across languages and contexts.[14]