Renpenning syndrome
intellectual disability that is characterized by small head size (microcephaly), long narrow face, short stature, small testes, and intellectual deficit which follows X-linked inheritance and presents most often in males
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Renpenning syndrome
Summary
Renpenning syndrome is a developmental defect during embryogenesis[1]. It draws 16 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #135 of 308).[2]
Key Facts
- Renpenning syndrome's instance of is recorded as developmental defect during embryogenesis[3].
- Renpenning syndrome's instance of is recorded as rare disease[4].
- Renpenning syndrome's instance of is recorded as class of disease[5].
- Renpenning syndrome is a type of X-linked intellectual disability[6].
- Renpenning syndrome is a type of syndromic anorectal malformation[7].
- Renpenning syndrome is a type of multiple congenital anomalies/dysmorphic syndrome-intellectual disability[8].
- Renpenning syndrome is a type of X-linked recessive disease[9].
- Renpenning syndrome's symptoms and signs is recorded as short stature[10].
- Renpenning syndrome's ICD-9-CM is recorded as 759.89[11].
- Renpenning syndrome's NCI Thesaurus ID is recorded as C165533[12].
- Renpenning syndrome's health specialty is recorded as medical genetics[13].
- Renpenning syndrome's genetic association is recorded as PQBP1[14].
- Renpenning syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060179[15].
- Renpenning syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0060179[16].
- Renpenning syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_3242[17].
- Renpenning syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[18].
Why It Matters
Renpenning syndrome draws 16 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #135 of 308).[2] It is known by 23 alternative names across languages and contexts.[19]