2006 ICD-9-CM Volume 1 Diagnosis Codes Home > Congenital Anomalies 740-759 > Other Congenital Musculoskeletal Anomalies 756.* > 2006 ICD-9-CM Diagnosis 756.0
Congenital anomalies of skull and face bonesView the most recent version of ICD-9-CM 756.0 - Premature closure of one or more sutures of the skull.
- An autosomal dominant disorder characterized by acrocephaly, exophthalmos, hypertelorism, strabismus, parrot-beaked nose, and hypoplastic maxilla with relative mandibular prognathism.
- Abnormal increase in the interorbital distance due to overdevelopment of the lesser wings of the sphenoid.
- 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.
- 756.0 is a specific code that can be used to specify a diagnosis
- 756.0 contains 116 index entries
- View the ICD-9-CM Volume 1 756.* hierarchy
Alternate Terminology- Absence of skull bones
- Acrocephaly
- Congenital deformity of forehead
- Craniosynostosis
- Crouzon's disease
- Hypertelorism
- Imperfect fusion of skull
- Oxycephaly
- Platybasia
- Premature closure of cranial sutures
- Tower skull
- Trigonocephaly
756.0 Excludes - acrocephalosyndactyly [Apert's syndrome] (755.55)
- dentofacial anomalies (524.0-524.9)
- skull defects associated with brain anomalies, such as:
Index entries containing 756.0:
- Abnormal, abnormality, abnormalities - see also Anomaly
- shape
- head (see also Anomaly, skull)
756.0
- size
- head (see also Anomaly, skull)
756.0
Absence (organ or part) (complete or partial)- bone (congenital) NEC 756.9
- skull
756.0
- calvarium, calvaria (skull)
756.0 - face
- bones NEC
756.0
- skull bone
756.0 Accessory (congenital)- face bone(s)
756.0 - frontonasal process
756.0 Acrobrachycephaly 756.0Acrocephaly 756.0Agenesis - see also Absence, by site, congenital- face
- bones NEC
756.0
- skull (bone)
756.0 Anomaly, anomalous (congenital) (unspecified type) 759.9- bone NEC 756.9
- cranium
756.0 - face
756.0 - frontal
756.0 - head
756.0 - skull
756.0
- face (any part) 744.9
- bone(s)
756.0
- forehead (see also Anomaly, skull)
756.0 - frontal bone (see also Anomaly, skull)
756.0 - head (see also Anomaly, skull)
756.0 - Pierre Robin
756.0 - skull (bone)
756.0 - specified type NEC
- bone(s) 756.9
- face
756.0 - skull
756.0
- face 744.89
- bone(s)
756.0
- skull (bone(s))
756.0
Bird- face
756.0 Brachycephaly 756.0Bulging fontanels (congenital) 756.0Caput- crepitus
756.0 Closure- cranial sutures, premature
756.0 - fontanelle, delayed
756.0 Craniofenestria (skull) 756.0Craniolacunia (skull) 756.0Cranioschisis 756.0Craniostenosis 756.0Craniosynostosis 756.0Crepitus- caput
756.0 Crouzon's disease (craniofacial dysostosis) 756.0Deficiency, deficient- craniofacial axis
756.0 Deficient - see also Deficiency- craniofacial axis
756.0 Deformity 738.9- cranium (acquired) 738.19
- congenital (see also Deformity, skull, congenital)
756.0
- forehead (acquired) 738.19
- congenital (see also Deformity, skull, congenital)
756.0
- frontal bone (acquired) 738.19
- congenital (see also Deformity, skull, congenital)
756.0
- head (acquired) 738.10
- congenital (see also Deformity, skull, congenital)
756.0
- Pierre Robin (congenital)
756.0 - skull (acquired) 738.19
- congenital
756.0- with
- due to intrauterine malposition and pressure 754.0
Delay, delayed- closure - see also Fistula
- cranial suture
756.0 - fontanel
756.0
Diastasis- cranial bones 733.99
- congenital
756.0
Dilatation- fontanel
756.0 Disease, diseased - see also Syndrome- Crouzon's (craniofacial dysostosis)
756.0 - Friedreich's
- facial hemihypertrophy
756.0
Distortion (congenital)- face bone(s)
756.0 - skull bone(s)
756.0 Duplication - see also Accessory- frontonasal process
756.0 Dysostosis- craniofacial
756.0 - mandibularis
756.0 - mandibulofacial, incomplete
756.0 Dysplasia - see also Anomaly- oculoauriculovertebral
756.0 Ecchordosis physaliphora 756.0Franceschetti's syndrome (mandibulofacial dysostosis) 756.0Fusion, fused (congenital)- cranial sutures, premature
756.0 - skull, imperfect
756.0 Goldenhar's syndrome (oculoauriculovertebral dysplasia) 756.0Greig's syndrome (hypertelorism) 756.0Hallermann-Streiff syndrome 756.0Hemihypertrophy (congenital) 759.89- cranial
756.0 Hyperostosis 733.99- skull 733.3
- congenital
756.0
Hypertelorism 756.0Hypoplasia, hypoplasis 759.89- bone NEC 756.9
- face
756.0 - malar
756.0 - skull (see also Hypoplasia, skull)
756.0
- face 744.89
- bone(s)
756.0
- skull (bone)
756.0 Idiot, idiocy (congenital) 318.2- oxycephalic
756.0 Imperfect- closure (congenital)
- skull
756.0
Impression, basilar 756.0Invagination- basilar
756.0 Lacunar skull 756.0Macrocephalia, macrocephaly 756.0Maldevelopment - see also Anomaly, by site- mastoid process
756.0 Megalocephalus, megalocephaly NEC 756.0Nager-de Reynier syndrome (dysostosis mandibularis) 756.0Oculoauriculovertebral dysplasia 756.0Ossification- fontanel
- defective or delayed
756.0 - premature
756.0
Oxycephaly, oxycephalic 756.0- syphilitic, congenital 090.0
Pierre Robin deformity or syndrome (congenital) 756.0Platybasia 756.0Premature - see also condition- closure
- cranial suture
756.0 - fontanel
756.0
Robin's syndrome 756.0Scaphocephaly 756.0Stenocephaly 756.0Sunken- fontanels
756.0 Syndrome - see also Disease- eyelid-malar-mandible
756.0 - first arch
756.0 - Franceschetti's (mandibulofacial dysostosis)
756.0 - Goldenhar's (oculoauriculovertebral dysplasia)
756.0 - Greig's (hypertelorism)
756.0 - Hallermann-Strieff
756.0 - incomplete
- mandibulofacial
756.0
- mandibulofacial dysostosis
756.0 - micrognathia-glossoptosis
756.0 - Nager-de Reynier (dysostosis mandibularis)
756.0 - OAV (oculoauriculovertebral dysplasia)
756.0 - Pierre Robin
756.0 - Robin's
756.0 - Treacher Collins' (incomplete mandibulofacial dysostosis)
756.0 Tower skull 756.0- with exophthalmos
756.0 Treacher Collins' syndrome (incomplete facial dysostosis) 756.0Trigonocephaly 756.0Turricephaly 756.0
|
|
|