Aplasia of skin of trunk
Sebaceous naevus
Aplasia of sweat gland
Absence of part of skin at birth
Gershoni Baruch Leibo syndrome
Sequelae of reproductive disorders
Aplasia of skin
Aplasia of skin (disorder)
Naevus sebaceous of Jadassohn
Congenital lymphangiectasis
Aplasia cutis in Johanson-Blizzard syndrome
ACC - Aplasia cutis congenita
Aplasia cutis congenita secondary to malformation syndrome (Type 9)
Aplasia cutis congenita
aplasia congenita cutis
Aplasia cutis congenita associated with fetus papyraceus (Type 5)
Aplasia cutis congenita in association with epidermolysis bullosa (Type 6)
Congenital anomaly of lymphatic structure of trunk
cutis aplasia
SCALP syndrome
ACC
Aplasia cutis in Trisomy 13 syndrome
Oculoectodermal syndrome
Aplasia cutis congenita (disorder)
APLASIA CUTIS CONGENITA, NONSYNDROMIC
Autosomal recessive aplasia cutis congenita of limb
Intestinal lymphangiectasia
aplasia cutis
congenita aplasia cuti
Aplasia cutis congenita due to underlying malformation (Type 4)
Aplasia cutis congenita with intestinal lymphangiectasia syndrome
Sebaceous naevus, central nervous system malformations, aplasia cutis congenita, limbal dermoid, pigmented naevus syndrome
cuti aplasia
Aplasia cutis congenita, naevus sebaceous syndrome
Nevus sebaceous
Hereditary disorder of lymphatic system
Aplasia cutis congenita due to teratogenic drug (Type 7)
Aplasia cutis congenita of trunk
Congenital lymphangiectasia
Aplasia of sudoriferous gland
Type 2 aplasia cutis
Congenital sequelae of disorders
Congenital absence of skin
Congenital absence of skin on scalp with limb-reduction anomaly
Congenital lymphangiectases
Didymosis aplasticosebacea
Sebaceous nevus
Microphthalmos due to Delleman syndrome
Delleman-Oorthuys syndrome
Aplasia cutis with myopia syndrome
Aplasia cutis congenita of limb
Aplasia cutis congenita with epibulbar dermoid syndrome
Aplasia cutis congenita associated with foetus papyraceus (Type 5)
Aplasia of eccrine gland
Epitheliogenesis imperfecta
Sebaceous nevus, central nervous system malformations, aplasia cutis congenita, limbal dermoid, pigmented nevus syndrome
Intestinal lymphangiectasis
Oculocerebrocutaneous syndrome
Aplasia cutis in Chromosome 4 short-arm deletion syndrome (Wolf-Hirschhorn)
Organoid naevus
Adams-Oliver syndrome
Bronspiegel Zelnick syndrome
Nevus sebaceous of Jadassohn
Aplasia cutis congenita, nevus sebaceous syndrome
Recessive aplasia cutis congenita of limbs
Dermoid cyst of eye proper
Toriello Lacassie Droste syndrome
Aplasia cutis congenita following intra-uterine infection (Type 8)
Naevus sebaceous
Organoid nevus

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.

How does Q84.8 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other specified congenital malformations of integument affect a person's functioning: body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.

What is the ICD-11 equivalent of Q84.8?

Q84.8 maps to the ICD-11 code: LC7Z (Structural developmental anomalies of the skin, unspecified).

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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.