gerodermia osteodysplastica

Summary

gerodermia osteodysplastica is a developmental defect during embryogenesis^[1]. It is known by 6 alternative names across languages and contexts.^[2]

Key Facts

• gerodermia osteodysplastica's instance of is recorded as developmental defect during embryogenesis^[3].
• gerodermia osteodysplastica's instance of is recorded as rare disease^[4].
• gerodermia osteodysplastica's instance of is recorded as class of disease^[5].
• gerodermia osteodysplastica is a type of cutis laxa^[6].
• gerodermia osteodysplastica is a type of dwarfism^[7].
• gerodermia osteodysplastica is a type of primary bone dysplasia with decreased bone density^[8].
• gerodermia osteodysplastica is a type of syndrome^[9].
• gerodermia osteodysplastica is a type of autosomal recessive disease^[10].
• gerodermia osteodysplastica's Commons category is recorded as Gerodermia osteodysplastica^[11].
• gerodermia osteodysplastica's ICD-9-CM is recorded as 759.89^[12].
• gerodermia osteodysplastica's health specialty is recorded as medical genetics^[13].
• gerodermia osteodysplastica's genetic association is recorded as GORAB^[14].
• gerodermia osteodysplastica's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_2078^[15].
• gerodermia osteodysplastica's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111266^[16].
• gerodermia osteodysplastica's exact match is recorded as http://identifiers.org/doid/DOID:0111266^[17].
• gerodermia osteodysplastica's on focus list of Wikimedia project is recorded as WikiProject Medicine^[18].

Why It Matters

gerodermia osteodysplastica is known by 6 alternative names across languages and contexts.^[2]