Other specified congenital malformations of skull and face bones

Preferred Label : Other specified congenital malformations of skull and face bones;

Inclusion CIM-10 : Platybasia; Absence of skull bone, congenital; Congenital deformity of forehead;

Diag associé à un acte (%) : 95.6;

Source : OMS;

Date de début : 01/01/1997;

Details

Origin ID

Q758;

UMLS CUI

C0478073;

Automatic exact mappings (from CISMeF team)
- Basilar invagination [MedDRA LLT]
- Congenital absence of skull bone (disorder) [SNOMED CT concept]
- Congenital deformity of forehead (disorder) [SNOMED CT concept]
- Platybasia [HPO term]
- Platybasia [MedDRA Preferred Term]
- Platybasia (disorder) [SNOMED CT concept]
- platybasia [MeSH Descriptor]
- platybasia [MeSH concept]
Orphanet concepts
- Acromelic frontonasal dysplasia [ORDO Disease]
- Alar cartilages hypoplasia-coloboma-telecanthus syndrome [ORDO Disease]
- Auriculocondylar syndrome [ORDO Disease]
- Craniolenticulosutural dysplasia [ORDO Disease]
- Craniosynostosis, Boston type [ORDO Disease]
- Delayed membranous cranial ossification [ORDO Disease]
- Enlarged parietal foramina [ORDO Disease]
- Frontofacionasal dysplasia [ORDO Disease]
- Frontonasal dysplasia [ORDO Disease]
- Frontorhiny [ORDO Disease]
- Maxillonasal dysplasia [ORDO Disease]
- Oculoauriculovertebral spectrum with radial defects [ORDO Disease]
- Osteosclerosis-developmental delay-craniosynostosis syndrome [ORDO Disease]
- Otomandibular syndrome [ORDO Disease]
- Primary basilar invagination [ORDO Disease]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]

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