2009 ICD-9-CM Diagnosis Code 756.0 : Congenital anomalies of skull and face bones

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2009 ICD-9-CM Diagnosis Code 756.0

Congenital anomalies of skull and face bones

Short description: ANOMAL SKULL/FACE BONES.
ICD-9-CM 756.0 is a billable medical code that can be used to indicate a diagnosis on a reimbursement claim, however, 756.0 should only be used for claims with a date of service on or before September 30, 2015. For claims with a date of service on or after October 1, 2015, use an equivalent ICD-10-CM code (or codes).
You are viewing the 2009 version of ICD-9-CM 756.0.
More recent version(s) of ICD-9-CM 756.0: 2010 2011 2012 2013 2014 2015.

Convert to ICD-10-CM: 756.0 converts approximately to:

2015/16 ICD-10-CM Q75.0 Craniosynostosis
Or:
2015/16 ICD-10-CM Q75.2 Hypertelorism
Or:
2015/16 ICD-10-CM Q75.9 Congenital malformation of skull and face bones, unspecified

Approximate Synonyms

Absence of skull bone
Absence, cranial bone
Anomaly of skull
Basilar skull invagination
Complex craniosynostosis
Congenital abnormality of skull and face bones
Congenital absence of cranial bone
Congenital deformity of facial bones
Congenital deformity of forehead
Congenital deformity of skull including facial bones
Congenital deformity, skull including facial bones
Craniosynostosis syndrome
Craniosynostosis, complex
Craniosynostosis, simple
Crouzon syndrome
Deformity of skull or facial bones, congenital
Delayed closure of anterior fontanel
Forehead deformity, congenital
Goldenhar syndrome
Hypertelorism
Invagination of basilar skull
Late closure of anterior fontanel
Macrocephaly
Macrocephaly, relative
Mandibulofacial dysostosis
Micrognathia-glossoptosis
Oculoauricular vertebral dysplasia
Oculomandibular dysostosis
Pierre Robin syndrome
Relative macrocephaly
Robin sequence
Robin syndrome
Simple craniosynostosis
Skull anomaly
Treacher collins syndrome

756.0 Excludes

acrocephalosyndactyly [Apert's syndrome] (755.55)
dentofacial anomalies (524.0-524.9)
skull defects associated with brain anomalies, such as:
- anencephalus (740.0)
- encephalocele (742.0)
- hydrocephalus (742.3)
- microcephalus (742.1)

Applies To

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

ICD-9-CM Volume 2 Index entries containing back-references to 756.0:

Abnormal, abnormality, abnormalities - see also Anomaly
- shape
  - cornea 743.41
  - gallbladder 751.69
  - gravid uterus 654.4
    - affecting fetus or newborn 763.89
    - causing obstructed labor 660.2
      - affecting fetus or newborn 763.1
  - head (see also Anomaly, skull) 756.0
  - organ or site, congenital NEC - see Distortion
- size
  - fetus, complicating delivery 653.5
    - causing obstructed labor 660.1
  - gallbladder 751.69
  - head (see also Anomaly, skull) 756.0
  - organ or site, congenital NEC - see Distortion
  - teeth 520.2
Absence (organ or part) (complete or partial)
- bone (congenital) NEC 756.9
  - marrow 284.9
    - acquired (secondary) 284.89
    - congenital 284.09
    - hereditary 284.09
    - idiopathic 284.9
  - skull 756.0
- calvarium, calvaria (skull) 756.0
- face
  - bones NEC 756.0
  - specified part NEC 744.89
- skull bone 756.0
  - with
    - anencephalus 740.0
    - encephalocele 742.0
    - hydrocephalus 742.3
      - with spina bifida (see also Spina bifida) 741.0
    - microcephalus 742.1
Accessory (congenital)
- face bone(s) 756.0
- frontonasal process 756.0
Acrobrachycephaly 756.0
Acrocephaly 756.0
Agenesis - see also Absence, by site, congenital
- face
  - bones NEC 756.0
  - specified part NEC 744.89
- skull (bone) 756.0
  - with
    - anencephalus 740.0
    - encephalocele 742.0
    - hydrocephalus 742.3
      - with spina bifida (see also Spina bifida) 741.0
    - microcephalus 742.1
Anomaly, anomalous (congenital) (unspecified type) 759.9
- bone NEC 756.9
  - ankle 755.69
  - arm 755.50
  - chest 756.3
  - cranium 756.0
  - face 756.0
  - finger 755.50
  - foot 755.67
  - forearm 755.50
  - frontal 756.0
  - head 756.0
  - hip 755.63
  - leg 755.60
  - lumbosacral 756.10
  - nose 748.1
  - pelvic girdle 755.60
  - rachitic 756.4
  - rib 756.3
  - shoulder girdle 755.50
  - skull 756.0
    - with
      - anencephalus 740.0
      - encephalocele 742.0
      - hydrocephalus 742.3
        with spina bifida (see also Spina bifida) 741.0
      - microcephalus 742.1
  - toe 755.66
- face (any part) 744.9
  - bone(s) 756.0
  - specified type NEC 744.89
- 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
  - with
    - anencephalus 740.0
    - encephalocele 742.0
    - hydrocephalus 742.3
      - with spina bifida (see also Spina bifida) 741.0
    - microcephalus 742.1
- specified type NEC
  - adrenal (gland) 759.1
  - alimentary tract (complete) (partial) 751.8
    - lower 751.5
    - upper 750.8
  - ankle 755.69
  - anus, anal (canal) 751.5
  - aorta, aortic 747.29
    - arch 747.21
  - appendix 751.5
  - arm 755.59
  - artery (peripheral) NEC (see also Anomaly, peripheral vascular system) 747.60
    - brain 747.81
    - coronary 746.85
    - eye 743.58
    - pulmonary 747.3
    - retinal 743.58
    - umbilical 747.5
  - auditory canal 744.29
    - causing impairment of hearing 744.02
  - bile duct or passage 751.69
  - bladder 753.8
    - neck 753.8
  - bone(s) 756.9
    - arm 755.59
    - face 756.0
    - leg 755.69
    - pelvic girdle 755.69
    - shoulder girdle 755.59
    - skull 756.0
      - with
        anencephalus 740.0
        encephalocele 742.0
        hydrocephalus 742.3
        with spina bifida (see also Spina bifida) 741.0
        microcephalus 742.1
  - brain 742.4
  - breast 757.6
  - broad ligament 752.19
  - bronchus 748.3
  - canal of Nuck 752.89
  - cardiac septal closure 745.8
  - carpus 755.59
  - cartilaginous 756.9
  - cecum 751.5
  - cervix 752.49
  - chest (wall) 756.3
  - chin 744.89
  - ciliary body 743.46
  - circulatory system 747.89
  - clavicle 755.51
  - clitoris 752.49
  - coccyx 756.19
  - colon 751.5
  - common duct 751.69
  - connective tissue 756.89
  - cricoid cartilage 748.3
  - cystic duct 751.69
  - diaphragm 756.6
  - digestive organ(s) or tract 751.8
    - lower 751.5
    - upper 750.8
  - duodenum 751.5
  - ear 744.29
    - auricle 744.29
      - causing impairment of hearing 744.02
    - causing impairment of hearing 744.09
    - inner (causing impairment of hearing) 744.05
    - middle, except ossicles 744.03
      - ossicles 744.04
  - ejaculatory duct 752.89
  - endocrine 759.2
  - epiglottis 748.3
  - esophagus 750.4
  - Eustachian tube 744.24
  - eye 743.8
    - lid 743.63
    - muscle 743.69
  - face 744.89
    - bone(s) 756.0
  - fallopian tube 752.19
  - fascia 756.89
  - femur 755.69
  - fibula 755.69
  - finger 755.59
  - foot 755.67
  - fovea centralis 743.55
  - gallbladder 751.69
  - Gartner's duct 752.89
  - gastrointestinal tract 751.8
  - genitalia, genital organ(s)
    - female 752.89
      - external 752.49
      - internal NEC 752.89
    - male 752.89
      - penis 752.69
      - scrotal transposition 752.81
  - genitourinary tract NEC 752.89
  - glottis 748.3
  - hair 757.4
  - hand 755.59
  - heart 746.89
    - valve NEC 746.89
      - pulmonary 746.09
  - hepatic duct 751.69
  - hydatid of Morgagni 752.89
  - hymen 752.49
  - integument 757.8
  - intestine (large) (small) 751.5
    - fixational type 751.4
  - iris 743.46
  - jejunum 751.5
  - joint 755.8
  - kidney 753.3
  - knee 755.64
  - labium (majus) (minus) 752.49
  - labyrinth, membranous 744.05
  - larynx 748.3
  - leg 755.69
  - lens 743.39
  - limb, except reduction deformity 755.8
    - lower 755.69
      - reduction deformity (see also Deformity, reduction, lower limb) 755.30
    - upper 755.59
      - reduction deformity (see also Deformity, reduction, upper limb) 755.20
  - lip 750.26
  - liver 751.69
  - lung (fissure) (lobe) 748.69
  - meatus urinarius 753.8
  - metacarpus 755.59
  - mouth 750.26
  - muscle 756.89
    - eye 743.69
  - musculoskeletal system, except limbs 756.9
  - nail 757.5
  - neck 744.89
  - nerve 742.8
    - acoustic 742.8
    - optic 742.8
  - nervous system 742.8
  - nipple 757.6
  - nose 748.1
  - organ NEC 759.89
    - of Corti 744.05
  - osseous meatus (ear) 744.03
  - ovary 752.0
  - oviduct 752.19
  - pancreas 751.7
  - parathyroid 759.2
  - patella 755.64
  - pelvic girdle 755.69
  - penis 752.69
  - pericardium 746.89
  - peripheral vascular system NEC (see also Anomaly, peripheral vascular system) 747.60
  - pharynx 750.29
  - pituitary 759.2
  - prostate 752.89
  - radius 755.59
  - rectum 751.5
  - respiratory system 748.8
  - rib 756.3
  - round ligament 752.89
  - sacrum 756.19
  - salivary duct or gland 750.26
  - scapula 755.59
  - sclera 743.47
  - scrotum 752.89
    - transposition 752.81
  - seminal duct or tract 752.89
  - shoulder girdle 755.59
  - site NEC 759.89
  - skin 757.39
  - skull (bone(s)) 756.0
    - with
      - anencephalus 740.0
      - encephalocele 742.0
      - hydrocephalus 742.3
        with spina bifida (see also Spina bifida) 741.0
      - microcephalus 742.1
  - specified organ or site NEC 759.89
  - spermatic cord 752.89
  - spinal cord 742.59
  - spine 756.19
  - spleen 759.0
  - sternum 756.3
  - stomach 750.7
  - tarsus 755.67
  - tendon 756.89
  - testis 752.89
  - thorax (wall) 756.3
  - thymus 759.2
  - thyroid (gland) 759.2
    - cartilage 748.3
  - tibia 755.69
  - toe 755.66
  - tongue 750.19
  - trachea (cartilage) 748.3
  - ulna 755.59
  - urachus 753.7
  - ureter 753.4
    - obstructive 753.29
  - urethra 753.8
    - obstructive 753.6
  - urinary tract 753.8
  - uterus 752.3
  - uvula 750.26
  - vagina 752.49
  - vascular NEC (see also Anomaly, peripheral vascular system) 747.60
    - brain 747.81
  - vas deferens 752.89
  - vein(s) (peripheral) NEC (see also Anomaly, peripheral vascular system) 747.60
    - brain 747.81
    - great 747.49
    - portal 747.49
    - pulmonary 747.49
  - vena cava (inferior) (superior) 747.49
  - vertebra 756.19
  - vulva 752.49
Bird
- face 756.0
Brachycephaly 756.0
Bulging fontanels (congenital) 756.0
Caput
- crepitus 756.0
Closure
- cranial sutures, premature 756.0
- fontanelle, delayed 756.0
Craniofenestria (skull) 756.0
Craniolacunia (skull) 756.0
Cranioschisis 756.0
Craniostenosis 756.0
Craniosynostosis 756.0
Crepitus
- caput 756.0
Crouzon's disease (craniofacial dysostosis) 756.0
Deficiency, 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
  - specified NEC 738.19
- Pierre Robin (congenital) 756.0
- skull (acquired) 738.19
  - congenital 756.0
    - with
      - anencephalus 740.0
      - encephalocele 742.0
      - hydrocephalus 742.3
        with spina bifida (see also Spina bifida) 741.0
      - microcephalus 742.1
    - 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
  - combined systemic or ataxia 334.0
  - facial hemihypertrophy 756.0
  - myoclonia 333.2
Distortion (congenital)
- face bone(s) 756.0
- skull bone(s) 756.0
  - with
    - anencephalus 740.0
    - encephalocele 742.0
    - hydrocephalus 742.3
      - with spina bifida (see also Spina bifida) 741.0
    - microcephalus 742.1
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 756.0
Franceschetti's syndrome (mandibulofacial dysostosis) 756.0
Fusion, fused (congenital)
- cranial sutures, premature 756.0
- skull, imperfect 756.0
Goldenhar's syndrome (oculoauriculovertebral dysplasia) 756.0
Greig's syndrome (hypertelorism) 756.0
Hallermann-Streiff syndrome 756.0
Hemihypertrophy (congenital) 759.89
- cranial 756.0
Hyperostosis 733.99
- skull 733.3
  - congenital 756.0
Hypertelorism 756.0
- orbit, orbital 376.41
Hypoplasia, hypoplasis 759.89
- bone NEC 756.9
  - face 756.0
  - malar 756.0
  - mandible 524.04
    - alveolar 524.74
  - marrow 284.9
    - acquired (secondary) 284.89
    - congenital 284.09
    - idiopathic 284.9
  - maxilla 524.03
    - alveolar 524.73
  - skull (see also Hypoplasia, skull) 756.0
- face 744.89
  - bone(s) 756.0
- skull (bone) 756.0
  - with
    - anencephalus 740.0
    - encephalocele 742.0
    - hydrocephalus 742.3
      - with spina bifida (see also Spina bifida) 741.0
    - microcephalus 742.1
Idiot, idiocy (congenital) 318.2
- oxycephalic 756.0
Imperfect
- closure (congenital)
  - alimentary tract NEC 751.8
    - lower 751.5
    - upper 750.8
  - atrioventricular ostium 745.69
  - atrium (secundum) 745.5
    - primum 745.61
  - branchial cleft or sinus 744.41
  - choroid 743.59
  - cricoid cartilage 748.3
  - cusps, heart valve NEC 746.89
    - pulmonary 746.09
  - ductus
    - arteriosus 747.0
    - Botalli 747.0
  - ear drum 744.29
    - causing impairment of hearing 744.03
  - endocardial cushion 745.60
  - epiglottis 748.3
  - esophagus with communication to bronchus or trachea 750.3
  - Eustachian valve 746.89
  - eyelid 743.62
  - face, facial (see also Cleft, lip) 749.10
  - foramen
    - Botalli 745.5
    - ovale 745.5
  - genitalia, genital organ(s) or system
    - female 752.89
      - external 752.49
      - internal NEC 752.89
      - uterus 752.3
    - male 752.89
      - penis 752.69
  - glottis 748.3
  - heart valve (cusps) NEC 746.89
  - interatrial ostium or septum 745.5
  - interauricular ostium or septum 745.5
  - interventricular ostium or septum 745.4
  - iris 743.46
  - kidney 753.3
  - larynx 748.3
  - lens 743.36
  - lip (see also Cleft, lip) 749.10
  - nasal septum or sinus 748.1
  - nose 748.1
  - omphalomesenteric duct 751.0
  - optic nerve entry 743.57
  - organ or site NEC - see Anomaly, specified type, by site
  - ostium
    - interatrial 745.5
    - interauricular 745.5
    - interventricular 745.4
  - palate (see also Cleft, palate) 749.00
  - preauricular sinus 744.46
  - retina 743.56
  - roof of orbit 742.0
  - sclera 743.47
  - septum
    - aortic 745.0
    - aorticopulmonary 745.0
    - atrial (secundum) 745.5
      - primum 745.61
    - between aorta and pulmonary artery 745.0
    - heart 745.9
    - interatrial (secundum) 745.5
      - primum 745.61
    - interauricular (secundum) 745.5
      - primum 745.61
    - interventricular 745.4
      - with pulmonary stenosis or atresia, dextraposition of aorta, and hypertrophy of right ventricle 745.2
      - in tetralogy of Fallot 745.2
    - nasal 748.1
    - ventricular 745.4
      - with pulmonary stenosis or atresia, dextraposition of aorta, and hypertrophy of right ventricle 745.2
      - in tetralogy of Fallot 745.2
  - skull 756.0
    - with
      - anencephalus 740.0
      - encephalocele 742.0
      - hydrocephalus 742.3
        with spina bifida (see also Spina bifida) 741.0
      - microcephalus 742.1
  - spine (with meningocele) (see also Spina bifida) 741.90
  - thyroid cartilage 748.3
  - trachea 748.3
  - tympanic membrane 744.29
    - causing impairment of hearing 744.03
  - uterus (with communication to bladder, intestine, or rectum) 752.3
  - uvula 749.02
    - with cleft lip (see also Cleft, palate, with cleft lip) 749.20
  - vitelline duct 751.0
Impression, basilar 756.0
Invagination
- basilar 756.0
Lacunar skull 756.0
Macrocephalia, macrocephaly 756.0
Maldevelopment - see also Anomaly, by site
- mastoid process 756.0
Megalocephalus, megalocephaly NEC 756.0
Nager-de Reynier syndrome (dysostosis mandibularis) 756.0
Oculoauriculovertebral dysplasia 756.0
Ossification
- fontanel
  - defective or delayed 756.0
  - premature 756.0
Oxycephaly, oxycephalic 756.0
- syphilitic, congenital 090.0
Pierre Robin deformity or syndrome (congenital) 756.0
Platybasia 756.0
Premature - see also condition
- closure
  - cranial suture 756.0
  - fontanel 756.0
  - foramen ovale 745.8
Robin's syndrome 756.0
Scaphocephaly 756.0
Stenocephaly 756.0
Sunken
- 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) 756.0
Trigonocephaly 756.0
Turricephaly 756.0

756

ICD9Data.com

756.1

ICD-9-CM codes are used in medical billing and coding to describe diseases, injuries, symptoms and conditions. ICD-9-CM 756.0 is one of thousands of ICD-9-CM codes used in healthcare. Although ICD-9-CM and CPT codes are largely numeric, they differ in that CPT codes describe medical procedures and services. Can't find a code? Start at the root of ICD-9-CM, check the 2009 ICD-9-CM Index or use the search engine at the top of this page to lookup any code.

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