mulibrey nanism
Human disease
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mulibrey nanism
Summary
mulibrey nanism is a developmental defect during embryogenesis[1]. It draws 56 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #128 of 308).[2]
Key Facts
- mulibrey nanism's instance of is recorded as developmental defect during embryogenesis[3].
- mulibrey nanism's instance of is recorded as rare disease[4].
- mulibrey nanism's instance of is recorded as class of disease[5].
- mulibrey nanism is a type of autosomal recessive disease[6].
- mulibrey nanism is a type of malformation syndrome with short stature[7].
- mulibrey nanism is a type of rare genetic developmental defect during embryogenesis[8].
- mulibrey nanism is a type of syndrome[9].
- mulibrey nanism's ICD-9-CM is recorded as 759.89[10].
- mulibrey nanism's NCI Thesaurus ID is recorded as C84906[11].
- mulibrey nanism's health specialty is recorded as rheumatology[12].
- mulibrey nanism's health specialty is recorded as medical genetics[13].
- mulibrey nanism's genetic association is recorded as TRIM37[14].
- mulibrey nanism's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0050436[15].
- mulibrey nanism's exact match is recorded as http://identifiers.org/doid/DOID:0050436[16].
- mulibrey nanism's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_2576[17].
- mulibrey nanism's on focus list of Wikimedia project is recorded as WikiProject Medicine[18].
Why It Matters
mulibrey nanism draws 56 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #128 of 308).[2] It has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[19] It is known by 14 alternative names across languages and contexts.[20]