Other congenital malformations of skull and face bones (Q75)
Clinical Information
Acanthosis Nigricans - A circumscribed melanosis consisting of a brown-pigmented, velvety verrucosity or fine papillomatosis appearing in the axillae and other body folds. It occurs in association with endocrine disorders, underlying malignancy, administration of certain drugs, or as in inherited disorder.
Choanal Atresia - A congenital abnormality that is characterized by a blocked CHOANAE, the opening between the nose and the NASOPHARYNX. Blockage can be unilateral or bilateral; bony or membranous.
Craniofacial Dysostosis - Autosomal dominant CRANIOSYNOSTOSIS with shallow ORBITS; EXOPHTHALMOS; and maxillary hypoplasia.
Exocrine Pancreatic Insufficiency - A malabsorption condition resulting from greater than 10% reduction in the secretion of pancreatic digestive enzymes (LIPASE; PROTEASES; and AMYLASE) by the EXOCRINE PANCREAS into the DUODENUM. This condition is often associated with CYSTIC FIBROSIS and with chronic PANCREATITIS.
Facial Asymmetry - Congenital or acquired asymmetry of the face.
Hypertelorism - Abnormal increase in the interorbital distance due to overdevelopment of the lesser wings of the sphenoid.
Mandibulofacial Dysostosis - A hereditary disorder occurring in two forms: the complete form (Franceschetti's syndrome) is characterized by a slant of the palpebral fissures, COLOBOMA of the lower lid, MICROGNATHIA and hypoplasia of the ZYGOMATIC ARCHES, and CONGENITAL MICROTIA. It is transmitted as an autosomal trait. The incomplete form (Treacher Collins syndrome) is characterized by the same anomalies in less pronounced degree. It occurs sporadically, but an autosomal dominant mode of transmission is suspected. (Dorland, 27th ed)
Osteopetrosis - Excessive formation of dense trabecular bone leading to pathological fractures; OSTEITIS; SPLENOMEGALY with infarct; ANEMIA; and extramedullary hemopoiesis (HEMATOPOIESIS, EXTRAMEDULLARY).
Osteosclerosis - An abnormal hardening or increased density of bone tissue.
Platybasia - A developmental deformity of the occipital bone and upper end of the cervical spine, in which the latter appears to have pushed the floor of the occipital bone upward. (Dorland, 27th ed)
Instructional Notations
Type 1 Excludes
A type 1 excludes note is a pure excludes note. It means "NOT CODED HERE!" An Excludes1 note indicates that the code excluded should never be used at the same time as the code above the Excludes1 note. An Excludes1 is used when two conditions cannot occur together, such as a congenital form versus an acquired form of the same condition.
- congenital malformation of face NOS Q18
- congenital malformation syndromes classified to Q87
- dentofacial anomalies [including malocclusion] M26
- musculoskeletal deformities of head and face Q67.0 Q67.4
- skull defects associated with congenital anomalies of brain such as:
- anencephaly Q00.0
- encephalocele Q01
- hydrocephalus Q03
- microcephaly Q02
Congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
Congenital malformations and deformations of the musculoskeletal system (Q65-Q79)
Q75 Other congenital malformations of skull and face bones
Q75.0 Craniosynostosis NEW CODE
Q75.00 Craniosynostosis unspecified NEW CODE
- Q75.001 Craniosynostosis unspecified, unilateral NEW CODE
- Q75.002 Craniosynostosis unspecified, bilateral NEW CODE
- Q75.009 Craniosynostosis unspecified NEW CODE
- Q75.01 Sagittal craniosynostosis NEW CODE
Q75.02 Coronal craniosynostosis NEW CODE
- Q75.021 Coronal craniosynostosis unilateral NEW CODE
- Q75.022 Coronal craniosynostosis bilateral NEW CODE
- Q75.029 Coronal craniosynostosis unspecified NEW CODE
- Q75.03 Metopic craniosynostosis NEW CODE
Q75.04 Lambdoid craniosynostosis NEW CODE
- Q75.041 Lambdoid craniosynostosis, unilateral NEW CODE
- Q75.042 Lambdoid craniosynostosis, bilateral NEW CODE
- Q75.049 Lambdoid craniosynostosis, unspecified NEW CODE
Q75.05 Multi-suture craniosynostosis NEW CODE
- Q75.051 Cloverleaf skull NEW CODE
- Q75.052 Pansynostosis NEW CODE
- Q75.058 Other multi-suture craniosynostosis NEW CODE
- Q75.08 Other single-suture craniosynostosis NEW CODE
- Q75.1 Craniofacial dysostosis
- Q75.2 Hypertelorism
- Q75.3 Macrocephaly
- Q75.4 Mandibulofacial dysostosis
- Q75.5 Oculomandibular dysostosis
- Q75.8 Other specified congenital malformations of skull and face bones
- Q75.9 Congenital malformation of skull and face bones, unspecified
Other congenital malformations of skull and face bones (Q75)