IMAGe syndrome
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IMAGe syndrome
Summary
IMAGe syndrome is a developmental defect during embryogenesis[1]. It is known by 8 alternative names across languages and contexts.[2]
Key Facts
- IMAGe syndrome's instance of is recorded as developmental defect during embryogenesis[3].
- IMAGe syndrome's instance of is recorded as rare disease[4].
- IMAGe syndrome's instance of is recorded as class of disease[5].
- IMAGe syndrome is a type of syndrome[6].
- IMAGe syndrome is a type of rare genetic adrenal disease[7].
- IMAGe syndrome is a type of Addison's disease[8].
- IMAGe syndrome is a type of syndromic urogenital tract malformation[9].
- IMAGe syndrome is a type of Slender bone dysplasia[10].
- IMAGe syndrome's ICD-9-CM is recorded as 759.89[11].
- IMAGe syndrome's NCI Thesaurus ID is recorded as C130988[12].
- IMAGe syndrome's genetic association is recorded as CDKN1C[13].
- IMAGe syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0050885[14].
- IMAGe syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0050885[15].
- IMAGe syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_85173[16].
- IMAGe syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[17].
Why It Matters
IMAGe syndrome is known by 8 alternative names across languages and contexts.[2]