Diagnosis Code

Q87.0 CONGEN MALFORM SYNDROMES PREDOM AFFECTING FACIAL APPEARANCE


Code Information

Diagnosis Code: Q87.0

Short Description: Congen malform syndromes predom affecting facial appearance

Long Description: Congenital malformation syndromes predominantly affecting facial appearance

The code Q87.0 is VALID for claim submission

Code Classification:

  • Congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
    • Other congenital malformations (Q80-Q89)
      • Oth congenital malform syndromes affecting multiple systems (Q87)
        • Q87.0 Congen malform syndromes predom affecting facial appearance

Code Version: 2022 ICD-10-CM


Synonyms

  • 10p partial monosomy syndrome
  • 16p12.1p12.3 triplication syndrome
  • 4q partial monosomy syndrome
  • 4q25 proximal deletion syndrome
  • Aase Smith type 1 syndrome
  • Abducens nerve palsy
  • Absence of clavicle
  • Acrocallosal syndrome
  • Acrocephalopolysyndactyly
  • Acrocephalopolysyndactyly type II
  • Acrocephalosyndactyly type I
  • Acromegaloid facial appearance syndrome
  • Acromelic frontonasal dysplasia
  • Acro-oto-ocular syndrome
  • Acrorenal mandibular syndrome
  • Aglossia-adactyly syndrome
  • AHDC1-related intellectual disability, obstructive sleep apnea, mild dysmorphism syndrome
  • Ambiguous genitalia
  • Anal atresia
  • Aneurysm osteoarthritis syndrome
  • Aortic arch anomaly, facial dysmorphism, intellectual disability syndrome
  • Arachnodactyly
  • Arachnodactyly
  • Arachnodactyly and intellectual disability with facial dysmorphism syndrome
  • Asymmetry of mandible
  • Auriculo-condylar syndrome
  • Autism and facial port-wine stain syndrome
  • Axonal neuropathy
  • Baraitser Winter cerebrofrontofacial syndrome
  • Basel Vanagaite Smirin Yosef syndrome
  • Bifid nose
  • Bilateral congenital dislocation of hip
  • Bilateral hearing loss
  • Binder syndrome
  • Blepharonasofacial malformation syndrome
  • BNAR syndrome
  • Bowing of upper limb
  • Brachycephaly
  • Brachytelephalangy, facial dysmorphism, Kallmann syndrome
  • Brain malformations, musculoskeletal abnormalities, facial dysmorphism, intellectual disability syndrome
  • Café au lait spots
  • Cardio-acral-facial syndrome
  • Cardio-facio-cutaneous syndrome
  • Central obesity
  • Cerebellar-facial-dental syndrome
  • Cerebrofacioarticular syndrome
  • Cerebro-facio-thoracic dysplasia
  • Cerebrooculonasal syndrome
  • Char syndrome
  • Charlie M syndrome
  • CHD3-related developmental delay, speech delay, intellectual disability, abnormalities of vision, facial dysmorphism syndrome
  • Chronic deafness
  • Cleft lip and palate, craniofacial dysmorphism, congenital heart defect, hearing loss syndrome
  • Cleft mandible
  • CODAS syndrome
  • Combined immunodeficiency with faciooculoskeletal anomalies syndrome
  • Congenital anomaly of aortic arch AND/OR descending aorta
  • Congenital asymmetry of jaw
  • Congenital atrophy of optic nerve
  • Congenital atrophy of optic nerve
  • Congenital bowing of long bone
  • Congenital cleft nose
  • Congenital conductive hearing loss
  • Congenital corneal dystrophy
  • Congenital corneal dystrophy
  • Congenital cubitus valgus
  • Congenital deformity of bone of forearm
  • Congenital diaphragmatic hernia
  • Congenital dislocation of left hip
  • Congenital dislocation of right hip
  • Congenital disorder of facial nerve
  • Congenital disorder of facial nerve
  • Congenital disorder of facial nerve
  • Congenital facial asymmetry
  • Congenital facial nerve palsy
  • Congenital facial nerve palsy
  • Congenital facial nerve palsy
  • Congenital hydronephrosis
  • Congenital hypoplasia of ulna
  • Congenital hypotrichia
  • Congenital labioscrotal agenesis, cerebellar malformation, corneal dystrophy, facial dysmorphism syndrome
  • Congenital livedo reticularis
  • Congenital mandibular asymmetry
  • Congenital nonprogressive myopathy with Moebius and Robin sequences
  • Congenital omphalocele
  • Congenital sixth nerve palsy
  • Congenital stenosis of carotid artery
  • Congenital umbilical hernia
  • Connective tissue disorder due to lysyl hydroxylase-3 deficiency
  • Contracture with ectodermal dysplasia and orofacial cleft syndrome
  • Cortical blindness
  • Crane Heise syndrome
  • Craniodigital syndrome and intellectual disability syndrome
  • Craniofacial dysplasia osteopenia syndrome
  • Craniofacial dyssynostosis syndrome
  • Craniofaciofrontodigital syndrome
  • Craniofrontonasal dysplasia
  • Craniomicromelic syndrome
  • Cryptophthalmos syndrome
  • Cyclops
  • Cyclops hypognathus
  • Cyprus facial neuromusculoskeletal syndrome
  • Dandy-Walker syndrome
  • Dandy-Walker syndrome
  • Deafness and intellectual disability Martin Probst type syndrome
  • Deletion of part of chromosome 10
  • Deletion of part of chromosome 4
  • Deletion of part of chromosome 5
  • Deletion of part of long arm of chromosome 5
  • Developmental delay, facial dysmorphism syndrome due to MED13L deficiency
  • Developmental malformation of branchial arch
  • Developmental malformation of branchial arch
  • Dextrotransposition of aorta
  • Diencephalic mesencephalic junction dysplasia
  • Dislocation of hip and facial dysmorphism syndrome
  • Dobrow syndrome
  • DYRK1A-related intellectual disability syndrome
  • Dysplasia with defective mineralization
  • Ear, face and neck congenital anomalies
  • Early-onset epileptic encephalopathy, cortical blindness, intellectual disability, facial dysmorphism syndrome
  • Early-onset seizures, distal limb anomalies, facial dysmorphism, global developmental delay syndrome
  • Edinburgh malformation syndrome
  • Elbow joint deformity
  • Emery Nelson syndrome
  • Epiphyseal dysplasia, hearing loss, dysmorphism syndrome
  • Expressive dysphasia
  • Facial asymmetry
  • Facial dysmorphism, anorexia, cachexia, eye and skin anomalies syndrome
  • Facial dysmorphism, cleft palate, loose skin syndrome
  • Facial dysmorphism, conductive hearing loss, heart defect syndrome
  • Facial dysmorphism, developmental delay, behavioral abnormalities syndrome due to 10p11.21p12.31 microdeletion
  • Facial dysmorphism, immunodeficiency, livedo, short stature syndrome
  • Facial dysmorphism, lens dislocation, anterior segment abnormalities, spontaneous filtering bleb syndrome
  • Facial dysmorphism, macrocephaly, myopia, Dandy-Walker malformation syndrome
  • Facial milia, lobate tongue, lingual and labial frenula syndrome
  • Facio-auriculo-vertebral spectrum
  • Familial aplasia of the vermis
  • Familial omphalocele syndrome with facial dysmorphism
  • Filippi syndrome
  • Fine Lubinsky syndrome
  • First and second branchial arch syndrome
  • First arch syndrome
  • Flat face, microstomia, ear anomaly syndrome
  • Frank-Ter Haar syndrome
  • Freeman-Sheldon syndrome
  • Frontonasal dysplasia sequence
  • Frontonasal dysplasia sequence
  • Frontonasal dysplasia sequence
  • Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome
  • Fryns macrocephaly
  • Fryns Smeets Thiry syndrome
  • Fryns syndrome
  • Gabriele-de Vries syndrome
  • Goldberg Shprintzen megacolon syndrome
  • Goldenhar syndrome
  • Gollop syndrome
  • Gorlin-Chaudhry-Moss syndrome
  • Greig cephalopolysyndactyly syndrome
  • Grob's syndrome
  • Hadziselimovic syndrome
  • Hall Riggs syndrome
  • Hallermann Streiff like syndrome
  • Hallermann-Streiff syndrome
  • Hanhart's syndrome
  • Harrod syndrome
  • Hemifacial microsomia
  • Hip pathological dislocation
  • Holzgreve syndrome
  • Hypertelorism
  • Hypogonadotropic hypogonadism, severe microcephaly, sensorineural hearing loss, dysmorphism syndrome
  • Illum syndrome
  • Immuno-osseous dysplasia
  • Intellectual disability Buenos Aires type
  • Intellectual disability Wolff type
  • Intellectual disability, brachydactyly, Pierre Robin syndrome
  • Intellectual disability, cardiac anomalies, short stature, joint laxity syndrome
  • Intellectual disability, coarse face, macrocephaly, cerebellar hypotrophy syndrome
  • Intellectual disability, craniofacial dysmorphism, cryptorchidism syndrome
  • Intellectual disability, craniofacial dysmorphism, hypogonadism, diabetes mellitus syndrome
  • Intellectual disability, expressive aphasia, facial dysmorphism syndrome
  • Intellectual disability, facial dysmorphism syndrome due to SETD5 haploinsufficiency
  • Intellectual disability, facial dysmorphism, hand anomalies syndrome
  • Intellectual disability, obesity, brain malformation, facial dysmorphism syndrome
  • Intellectual disability, seizures, abnormal gait, facial dysmorphism syndrome
  • Intellectual disability, severe speech delay, mild dysmorphism syndrome
  • Internal carotid artery stenosis
  • Isolated hereditary congenital facial paralysis
  • Isotretinoin-like syndrome
  • Jawad syndrome
  • Joint contractures, developmental delay, Pierre Robin syndrome
  • Joubert syndrome
  • Joubert syndrome with orofaciodigital defect
  • Juberg Marsidi syndrome
  • Kagami Ogata syndrome
  • Kapur Toriello syndrome
  • Keipert syndrome
  • Keppen Lubinsky syndrome
  • King Denborough syndrome
  • Klippel-Feil anomaly, myopathy, facial dysmorphism syndrome
  • Klippel-Feil sequence
  • Klippel-Feil sequence
  • Koolen De Vries syndrome
  • Lamb Shaffer syndrome
  • Larsen-like syndrome B3GAT3 type
  • Lentiglobus
  • Lethal faciocardiomelic dysplasia
  • Lethal polymalformative syndrome Boissel type
  • Livedo reticularis
  • Lymphedema of lower extremity
  • Lymphedema, atrial septal defect, facial changes syndrome
  • McDonough syndrome
  • Megalocornea
  • Mehes syndrome
  • Melnick-Fraser syndrome
  • Menke Hennekam syndrome
  • Metopic ridging, ptosis, facial dysmorphism syndrome
  • Microcephaly, short stature, intellectual disability, facial dysmorphism syndrome
  • Microphthalmos due to Fryns syndrome
  • Microstomia
  • Microtia
  • Mietens syndrome
  • Miller syndrome
  • Moebius syndrome
  • Moebius syndrome, axonal neuropathy, hypogonadotropic hypogonadism syndrome
  • Mohr syndrome
  • Mowat-Wilson syndrome
  • Moyamoya angiopathy, short stature, facial dysmorphism, hypergonadotropic hypogonadism syndrome
  • Moyamoya disease
  • Mucopolysaccharidosis-like plus disease
  • Multicentric osteolysis nodulosis arthropathy spectrum
  • Multiple malformation syndrome with facial defects as major feature
  • Multiple malformation syndrome with facial-limb defects as major feature
  • Multiple malformation syndrome, moderate short stature, facial
  • Multiple malformation syndrome, small stature, without skeletal dysplasia
  • Nager syndrome
  • Night blindness
  • Night blindness, skeletal anomalies, dysmorphism syndrome
  • Nijmegen breakage syndrome-like disorder
  • Non-specific syndromic intellectual disability
  • Obstructive sleep apnea syndrome
  • Occipital encephalocele
  • Oculoauriculofrontonasal syndrome
  • Oculo-auriculo-vertebral spectrum
  • Oculocerebrodental syndrome
  • Oculocerebrofacial syndrome Kaufman type
  • Oculodento-osseous dysplasia
  • Oculomaxillofacial dysostosis
  • Oculo-palato-digital syndrome
  • Ogden syndrome
  • Okamoto syndrome
  • Ophthalmomandibulomelic dysplasia
  • Opocephalus
  • Oral-facial-digital syndrome
  • Oro-facial digital syndrome type 1
  • Oro-facial digital syndrome type 10
  • Oro-facial digital syndrome type 11
  • Oro-facial digital syndrome type 12
  • Oro-facial digital syndrome type 13
  • Oro-facial digital syndrome type 14
  • Oro-facial digital syndrome type 5
  • Oro-facial digital syndrome type 8
  • Orofacial-digital syndrome III
  • Orofacial-digital syndrome IV
  • Oromandibular-limb hypogenesis spectrum
  • Oromandibular-limb hypogenesis spectrum
  • Otocephalic syndrome
  • Otofaciocervical syndrome
  • Otopalatodigital syndrome spectrum disorder
  • Otopalatodigital syndrome spectrum disorder
  • Oto-palato-digital syndrome, type I
  • Oto-palato-digital syndrome, type II
  • Palatal anomalies, widely spaced teeth, facial dysmorphism, developmental delay syndrome
  • Pallister W syndrome
  • Pathological dislocation of left hip
  • PDE4D haploinsufficiency syndrome
  • Pelviscapular dysplasia
  • Peripheral axonal neuropathy
  • Perlman syndrome
  • Pierpont syndrome
  • Pierre Robin sequence faciodigital anomaly syndrome
  • Pilotto syndrome
  • Plagiocephaly
  • Poliosis
  • Port-wine stain of skin
  • Postaxial polydactyly, anterior pituitary anomalies, facial dysmorphism syndrome
  • Potter's facies
  • Prieto Badia Mulas syndrome
  • Proximal deletion of long arm of chromosome 4
  • Pseudoaminopterin syndrome
  • Pseudopapilledema
  • PYCR2-related microcephaly, progressive leukoencephalopathy
  • Ramos Arroyo syndrome
  • Renal agenesis
  • RIDDLE syndrome
  • Right aortic arch
  • Robin sequence
  • Robin sequence
  • Robin sequence
  • Robin sequence
  • Robin sequence
  • Robin sequence
  • Robin sequence
  • Robin sequence and oligodactyly syndrome
  • Roifman syndrome
  • Rozin Hertz Goodman syndrome
  • Ruvalcaba syndrome
  • Sanjad Sakati syndrome
  • SATB2-associated syndrome
  • SCARF syndrome
  • Schilbach Rott syndrome
  • Seaver Cassidy syndrome
  • Severe intellectual disability, hypotonia, strabismus, coarse face, planovalgus syndrome
  • Severe intellectual disability, poor language, strabismus, grimacing face, long fingers syndrome
  • Severe intellectual disability, short stature, behavioral abnormalities, facial dysmorphism syndrome
  • Severe X-linked intellectual disability Gustavson type
  • Short stature, onychodysplasia, facial dysmorphism, hypotrichosis syndrome
  • Short stature, Pierre Robin sequence, cleft mandible, hand anomalies, clubfoot syndrome
  • Short stature, unique facies, enamel hypoplasia, progressive joint stiffness, high-pitched voice syndrome
  • Short ulna, dysmorphism, hypotonia, intellectual disability syndrome
  • Sixth cranial nerve finding
  • Sleep apnea
  • Sonoda syndrome
  • Speech delay
  • Speech delay
  • Spherophakia
  • Spondylometaphyseal dysplasia, bowed forearms, facial dysmorphism syndrome
  • STAG1-related intellectual disability, facial dysmorphism, gastroesophageal reflux syndrome
  • STAR syndrome
  • Steel syndrome
  • Steinfeld syndrome
  • Syndromic multisystem autoimmune disease due to ITCH deficiency
  • Syndromic X-linked intellectual disability type 11
  • TARP syndrome
  • Teebi Shaltout syndrome
  • Telecanthus
  • Temple syndrome
  • Temtamy syndrome
  • Thakker Donnai syndrome
  • Thin ribs, tubular bones, dysmorphism syndrome
  • THOC6-related developmental delay-microcephaly-facial dysmorphism syndrome
  • TMEM94-associated congenital heart defect, facial dysmorphism, developmental delay syndrome
  • Tongue absent
  • Toriello Carey syndrome
  • Townes syndrome
  • Van den Ende-Gupta syndrome
  • Velofacioskeletal syndrome
  • Ventricular extrasystoles with syncope, perodactyly and Robin sequence syndrome
  • WAC-related facial dysmorphism, developmental delay, behavioral abnormalities syndrome
  • WAC-related facial dysmorphism, developmental delay, behavioral abnormalities syndrome
  • Weill-Marchesani syndrome
  • White forelock with malformations syndrome
  • Wildervanck syndrome
  • Wilson Turner syndrome
  • Witteveen Kolk syndrome
  • X-linked female restricted facial dysmorphism, short stature, choanal atresia, intellectual disability
  • X-linked intellectual disability and epilepsy with progressive joint contracture and facial dysmorphism syndrome
  • X-linked intellectual disability and hypotonia with facial dysmorphism and aggressive behavior syndrome
  • X-linked intellectual disability hypotonic face syndrome
  • X-linked intellectual disability Nascimento type
  • X-linked intellectual disability Seemanova type
  • X-linked intellectual disability Siderius type
  • X-linked intellectual disability Stevenson type
  • X-linked intellectual disability Stoll type
  • X-linked intellectual disability with cubitus valgus and dysmorphism syndrome
  • X-linked intellectual disability with plagiocephaly syndrome
  • X-linked intellectual disability, global development delay, facial dysmorphism, sacral caudal remnant syndrome
  • X-linked sensorineural hearing loss
  • Zechi Ceide syndrome

Diagnostic Related Group(s)

The code Q87.0 is grouped in the following Diagnostic Related Group(s) (MS-DRG v39.0)
  • Other Musculoskeletal System And Connective Tissue Diagnoses With Mcc (564)
  • Other Musculoskeletal System And Connective Tissue Diagnoses With Cc (565)
  • Other Musculoskeletal System And Connective Tissue Diagnoses Without Cc/mcc (566)

References to Index of Diseases and Injuries

The code Q87.0 has the following ICD-10-CM references to the Index of Diseases and Injuries
  • Inclusion Terms:
    • Acrocephalopolysyndactyly
    • Acrocephalosyndactyly [Apert]
    • Cryptophthalmos syndrome
    • Cyclopia
    • Goldenhar syndrome
    • Moebius syndrome
    • Oro-facial-digital syndrome
    • Robin syndrome
    • Whistling face

Crosswalk Information

ICD-10 Code ICD-9 Code ICD-9 Description
Q87.0 Right Arrow 755.55 Acrocephalosyndactyly
756.0 Anomal skull/face bones

This ICD-10 to ICD-9 data is based on the 2018 General Equivalency Mapping (GEM) files published by the Centers for Medicare & Medicaid Services (CMS) for informational purposes only. The data is not an ICD-10 conversion tool and doesn’t guarantee clinical accuracy.

Similar Codes

ICD-10 Code ICD-10 Description
Q87 Other specified congenital malformation syndromes affecting multiple systems
Q87.1 Congenital malformation syndromes predominantly associated with short stature
Q87.11 Prader-Willi syndrome
Q87.19 Other congenital malformation syndromes predominantly associated with short stature
Q87.2 Congenital malformation syndromes predominantly involving limbs
Q87.3 Congenital malformation syndromes involving early overgrowth
Q87.4 Marfan syndrome
Q87.40 Marfan syndrome, unspecified
Q87.41 Marfan syndrome with cardiovascular manifestations
Q87.410 Marfan syndrome with aortic dilation
Q87.418 Marfan syndrome with other cardiovascular manifestations
Q87.42 Marfan syndrome with ocular manifestations
Q87.43 Marfan syndrome with skeletal manifestation
Q87.5 Other congenital malformation syndromes with other skeletal changes
Q87.8 Other specified congenital malformation syndromes, not elsewhere classified
Q87.81 Alport syndrome
Q87.82 Arterial tortuosity syndrome
Q87.83 Bardet-Biedl syndrome
Q87.84 Laurence-Moon syndrome
Q87.85 MED13L syndrome
Q87.89 Other specified congenital malformation syndromes, not elsewhere classified


This page was last updated on: 10/1/2023