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osteopathia striata with cranial sclerosis

Disease Summary
Associated Targets (1)
Tbio

1


GARD Rare
Mondo Description Osteopathia striata with cranial sclerosis (OS-CS) is a bone dysplasia characterized by longitudinal striations of the metaphyses of the long bones, sclerosis of the craniofacial bones, macrocephaly, cleft palate and hearing loss.
Uniprot Description An X-linked dominant sclerosing bone dysplasia that presents in females with macrocephaly, cleft palate, facial palsy, conductive hearing loss, mild learning disabilities, sclerosis of the long bones and skull. Longitudinal striations are visible on radiographs of the long bones, pelvis, and scapulae (osteopathia striata). In males this entity is usually associated with fetal or neonatal lethality. Occasional surviving males have, in addition to hyperostosis, cardiac, intestinal, and genitourinary malformations.
Disease Ontology Description An osteosclerosis characterized by longitudinal striations of the metaphyses of the long bones, sclerosis of the craniofacial bones, macrocephaly, cleft palate and hearing loss in females and fetal or neonatal lethality in males that has material_basis_in mutation in the AMER1 gene on chromosome Xq11.
Mondo Term and Equivalent IDs
MONDO:0010310:  osteopathia striata with cranial sclerosis
EFO:0005834: 
GARD:0004148: 
MESH:C536053: 
Orphanet:2780: 
SCTID:254129003: 
UMLS:C0432268: