Q84.8
BillableOther specified congenital malformations of integument
Other specified congenital malformations of integument
Status
Billable / Specific
Parent Code
Q84Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Aplasia cutis congenita
Excludes 2
Conditions not included here, but the patient may have both
- inborn errors of metabolism (E70-E88)
Also Known As / Clinical Terms
SNOMED CT
- Adams-Oliver syndrome34748004
- Congenital absence of skin on scalp with limb-reduction anomaly34748004
- Type 2 aplasia cutis34748004
- ACC - Aplasia cutis congenita35484002
- Aplasia cutis congenita35484002
- Congenital absence of skin35484002
- Cutis aplasia35484002
- Epitheliogenesis imperfecta35484002
- Intestinal lymphangiectasia197260007
- Intestinal lymphangiectasis197260007
- Aplasia of skin254237003
- Congenital anomaly of lymphatic structure of trunk363031002
- Congenital sequelae of disorders363042006
- Hereditary disorder of lymphatic system363190001
- Sequelae of reproductive disorders363305005
- Aplasia cutis congenita due to underlying malformation (Type 4)403548007
- Aplasia cutis congenita associated with fetus papyraceus (Type 5)403549004
- Aplasia cutis congenita associated with foetus papyraceus (Type 5)403549004
- Aplasia cutis congenita in association with epidermolysis bullosa (Type 6)403550004
- Aplasia cutis congenita due to teratogenic drug (Type 7)403551000
- Aplasia cutis congenita following intra-uterine infection (Type 8)403552007
- Aplasia cutis congenita secondary to malformation syndrome (Type 9)403553002
- Delleman-Oorthuys syndrome403554008
- Oculocerebrocutaneous syndrome403554008
- Aplasia cutis in Trisomy 13 syndrome403756008
- Aplasia cutis in Chromosome 4 short-arm deletion syndrome (Wolf-Hirschhorn)403757004
- Aplasia cutis in Johanson-Blizzard syndrome403763008
- Naevus sebaceous707136009
- Naevus sebaceous of Jadassohn707136009
- Nevus sebaceous707136009
- Nevus sebaceous of Jadassohn707136009
- Organoid naevus707136009
- Organoid nevus707136009
- Sebaceous naevus707136009
- Sebaceous nevus707136009
- Aplasia cutis with myopia syndrome720499004
- Gershoni Baruch Leibo syndrome720499004
- Aplasia cutis congenita with intestinal lymphangiectasia syndrome720500008
- Bronspiegel Zelnick syndrome720500008
- Autosomal recessive aplasia cutis congenita of limb723500009
- Recessive aplasia cutis congenita of limbs723500009
- Aplasia cutis congenita with epibulbar dermoid syndrome723554006
- Oculoectodermal syndrome723554006
- Toriello Lacassie Droste syndrome723554006
- SCALP syndrome774208009
- Sebaceous naevus, central nervous system malformations, aplasia cutis congenita, limbal dermoid, pigmented naevus syndrome774208009
- Sebaceous nevus, central nervous system malformations, aplasia cutis congenita, limbal dermoid, pigmented nevus syndrome774208009
- Aplasia cutis congenita, naevus sebaceous syndrome774209001
- Aplasia cutis congenita, nevus sebaceous syndrome774209001
- Didymosis aplasticosebacea774209001
- Congenital lymphangiectases788292004
- Congenital lymphangiectasia788292004
- Congenital lymphangiectasis788292004
- Dermoid cyst of eye proper830036006
- Aplasia cutis congenita of limb838362006
- Microphthalmos due to Delleman syndrome1003369001
- Aplasia cutis congenita of trunk1144556009
- Aplasia of skin of trunk1144556009
- Aplasia of sudoriferous gland1144873002
- Aplasia of sweat gland1144873002
- Aplasia of eccrine gland1144874008
UMLS
- ACCC0282160
- ACC - Aplasia cutis congenitaC0282160
- APLASIA CUTIS CONGENITA, NONSYNDROMICC0282160
- Absence of part of skin at birthC0282160
- Aplasia Cutis CongenitaC0282160
- Aplasia Cutis Congenita, NonsyndromicC0282160
- Aplasia cutisC0282160
- Aplasia cutis congenitaC0282160
- Aplasia cutis congenita (disorder)C0282160
- Aplasia of skinC0282160
- Aplasia of skin (disorder)C0282160
- Congenital absence of skinC0282160
- Cutis aplasiaC0282160
- Epitheliogenesis imperfectaC0282160
- aplasia congenita cutisC0282160
- aplasia cutisC0282160
- aplasia cutis congenitaC0282160
- congenita aplasia cutiC0282160
- cuti aplasiaC0282160
- cutis aplasiaC0282160
- Other specified congenital malformations of integumentC0478090
Frequently Asked Questions
What is the ICD-10 code for other specified congenital malformations of integument?
The ICD-10-CM code for other specified congenital malformations of integument is Q84.8. The full clinical description is "Other specified congenital malformations of integument". Q84.8 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code Q84.8 mean?
ICD-10-CM code Q84.8 represents "Other specified congenital malformations of integument". It is classified under Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities and is a billable/specific code that can be used on a claim.
Is Q84.8 a billable code?
Yes, Q84.8 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Q84.8 in?
Q84.8 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).
What SNOMED CT codes does Q84.8 map to?
Q84.8 maps to 32 SNOMED CT concepts: 35484002, 34748004, 403549004, 403551000, 403548007, and 27 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for Q84.8?
Q84.8 is linked to 2 UMLS Concept Unique Identifiers: C0282160, C0478090. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.