Disease #02151 (OSCS (osteopathia striata with cranial sclerosis (OSCS)), OMIM:300373)

Official abbreviation OSCS
Name osteopathia striata with cranial sclerosis (OSCS)
OMIM ID 300373
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene FAM123B
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Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00100437 - - - F no Italy caucasian - 0 - - OSCS Clinical diagnosis of OCSC: cleft palat, hearing loss, macrocephaly, facial features with frontal bossing, hypertelorism, epicanthus, longitudinal sclerotic striations of the long bones metaphysis FAM123B FAM123B 1 1 Eva Trevisson
00306203 101 - - M - China - - - - - OSCS - AMER2 AMER2 1 1 Sha Hong
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