Wiedemann-Rautenstrauch syndrome
very rare disorder with features of premature aging recognizable at birth, decreased subcutaneous fat, hypotrichosis, relative macrocephaly and dysmorphism
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Wiedemann-Rautenstrauch syndrome
Summary
Wiedemann-Rautenstrauch syndrome is a developmental defect during embryogenesis[1]. It has Wikipedia articles in 9 language editions, a strong signal of global cultural recognition.[2]
Key Facts
- Wiedemann-Rautenstrauch syndrome's instance of is recorded as developmental defect during embryogenesis[3].
- Wiedemann-Rautenstrauch syndrome's instance of is recorded as class of disease[4].
- Hans-Rudolf Wiedemann is named after Wiedemann-Rautenstrauch syndrome[5].
- Wiedemann-Rautenstrauch syndrome is a type of progeroid syndrome[6].
- Wiedemann-Rautenstrauch syndrome is a type of genetic syndromic intellectual disability[7].
- Wiedemann-Rautenstrauch syndrome is a type of secondary ectropion[8].
- Wiedemann-Rautenstrauch syndrome is a type of genetic lipodystrophy[9].
- Wiedemann-Rautenstrauch syndrome is a type of multiple congenital anomalies/dysmorphic syndrome-intellectual disability[10].
- Wiedemann-Rautenstrauch syndrome is a type of developmental anomaly of metabolic origin[11].
- Wiedemann-Rautenstrauch syndrome is a type of malformation syndrome with skin/mucosae involvement[12].
- Wiedemann-Rautenstrauch syndrome's ICD-9-CM is recorded as 259.8[13].
- Wiedemann-Rautenstrauch syndrome's NCI Thesaurus ID is recorded as C121565[14].
- Wiedemann-Rautenstrauch syndrome's health specialty is recorded as endocrinology[15].
- Wiedemann-Rautenstrauch syndrome's genetic association is recorded as POLR3A[16].
- Wiedemann-Rautenstrauch syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_3455[17].
Why It Matters
Wiedemann-Rautenstrauch syndrome has Wikipedia articles in 9 language editions, a strong signal of global cultural recognition.[2] It is known by 6 alternative names across languages and contexts.[18]