Fuhrmann syndrome
Fuhrmann syndrome is mainly characterized by bowing of the femora, aplasia or hypoplasia of the fibulae and poly-, oligo-, and syndactyly
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Fuhrmann syndrome
Summary
Fuhrmann syndrome is a hereditary disorder[1]. It is known by 8 alternative names across languages and contexts.[2]
Key Facts
- Fuhrmann syndrome's instance of is recorded as hereditary disorder[3].
- Fuhrmann syndrome's instance of is recorded as head and neck disease[4].
- Fuhrmann syndrome's instance of is recorded as developmental defect during embryogenesis[5].
- Fuhrmann syndrome's instance of is recorded as class of disease[6].
- Fuhrmann syndrome is a type of bone development disease[7].
- Fuhrmann syndrome is a type of syndrome with limb duplication, polydactyly, syndactyly, and/or hyperphalangy[8].
- Fuhrmann syndrome is a type of syndrome with limb reduction defects[9].
- Fuhrmann syndrome is a type of orofacial clefting syndrome[10].
- Fuhrmann syndrome is a type of genetic disease[11].
- Fuhrmann syndrome is a type of autosomal recessive disease[12].
- Fuhrmann syndrome's health specialty is recorded as medical genetics[13].
- Fuhrmann syndrome's genetic association is recorded as WNT7A[14].
- Fuhrmann syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0090067[15].
- Fuhrmann syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0090067[16].
- Fuhrmann syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_2854[17].
- Fuhrmann syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[18].
Why It Matters
Fuhrmann syndrome is known by 8 alternative names across languages and contexts.[2]