MIRAGE (myelodysplasia, infection, restriction of growth, adrenal hypoplasia, genital anomalies, enteropathy) syndrome
Congenital anomaly of male genital system (disorder)
Congenital small adrenal gland
Centronuclear myopathy
Congenital anomaly of genital organ
Corpus callosum agenesis, abnormal genitalia syndrome
Urban Rogers Meyer syndrome
Frontonasal dysplasia with alopecia and genital abnomality
Arachnodactyly
RAB18 deficiency
Congenital genital malformation male
Syndactyly, telecanthus, anogenital and renal malformation syndrome
Atresia ani
BILU (B-cell immunodeficiency, limb, urogenital) syndrome
Median cleft face syndrome
Myotubular myopathy
46,XY disorder of sex development due to environmental chemical exposure
WAGR (Wilms tumor, aniridia, genitourinary anomalies and mental retardation) syndrome
Aproctia
PELVIS (Perineal haemangioma, external genitalia malformation, lipomyelomeningocele, vesicorenal abnormality, imperforate anus) syndrome
Aplasia of bone of forearm
IMAGe syndrome
MIRAGE syndrome
Perineal hemangioma, external genitalia malformation, lipomyelomeningocele, vesicorenal abnormality, imperforate anus syndrome
RAB18, member RAS oncogene family deficiency
Genitopatellar syndrome
MYRF-related cardiac urogenital syndrome
Pseudohermaphroditism with intellectual disability syndrome
Absent radius, anogenital anomalies syndrome
Congenital deformity of genital organ
Hoffman syndrome due to TOP2B deficiency
Congenital anomaly of male genital organ
Agammaglobulinaemia due to TOP2B mutation
Congenital genital organ anomalies
CAH - Congenital adrenal hypoplasia
Spider finger
11p partial monosomy syndrome
Acro-cardio-facial syndrome
STAR (syndactyly, telecanthus, anogenital, renal malformation) syndrome
Lobster claw hand
ALX4 (human aristaless-like 4) related frontonasal dysplasia with alopecia and genital anomaly
Autosomal recessive facio-digito-genital syndrome
STAR syndrome
B-cell immunodeficiency, limb anomaly, urogenital malformation syndrome
Cardiac urogenital syndrome
Hydrometrocolpos, postaxial polydactyly, and congenital heart malformation
Congenital male urogenital anomaly
Frontonasal dysplasia with alopecia and genital anomaly syndrome
Chromosome 11p13 deletion syndrome
Cleft palate, cardiac defect, genital anomalies, and ectrodactyly
Myelin regulatory factor-related cardiac urogenital syndrome
Spondylocostal dysostosis with anal atresia and genitourinary malformation syndrome
Congenital absence of radius
Congenital arachnodactyly
ACFS - acrocardiofacial syndrome
Acrocardiofacial syndrome
Congenital hypoplasia of adrenal gland
WAGR syndrome
X-linked myotubular myopathy, abnormal genitalia syndrome
Agenesis of corpus callosum and abnormal genitalia syndrome
Aplasia of bone of radius and/or ulna
PELVIS (perineal hemangioma, external genitalia malformation, lipomyelomeningocele, vesicorenal abnormality, imperforate anus) syndrome
46,XY disorder of sex development due to isolated 17,20-lyase deficiency
Aplasia of radius
Proud Levine Carpenter syndrome
Hand-foot-uterus syndrome
Congenital atresia of anus
Congenital deformity of male genital organ
McKusick Kaufman syndrome
Congenital adrenal hypoplasia
Verloes Gillerot Fryns syndrome
Congenital anomaly of male urogenital tract
Telecanthus
Deafness, genital anomaly, metacarpal and metatarsal synostosis syndrome
Dysmorphism, short stature, deafness, disorder of sex development syndrome
Waters West syndrome
X-linked lissencephaly with ambiguous genitalia
46,XY disorder of sex development
Imperforate anus
Myelodysplasia, infection, restriction of growth, adrenal hypoplasia, genital phenotypes, enteropathy syndrome
Deletion of part of chromosome 11
Craniofrontonasal dysplasia with alopecia and hypogonadism
Agammaglobulinemia due to TOP2B mutation
Disorder of sex development with intellectual disability syndrome
Facio-digito-genital syndrome Kuwait type
Congenital urogenital anomaly
Aphalangy, hemivertebra, urogenital, intestinal dysgenesis syndrome
CCGE - cleft palate, cardiac defect, genital anomalies, ectrodactyly syndrome
Congenital anomaly of male genital system
Hand-foot-genital syndrome
Congenital cleft hand
Xq28 contiguous gene deletion syndrome
Congenital obstructive azoospermia
Short stature co-occurrent and due to endocrine disorder
Casamassima Morton Nance syndrome
Teebi Naguib Alawadi syndrome
Myelodysplasia, infection, restriction of growth, adrenal hypoplasia, genital anomalies, enteropathy syndrome
BILU syndrome
Lethal haemolytic anaemia and genital anomaly syndrome
X-linked lissencephaly with abnormal genitalia syndrome
X-linked lissencephaly with agenesis of corpus callosum and genital anomaly syndrome
Frontonasal dysplasia sequence
Microcephaly, corpus callosum agenesis, abnormal genitalia syndrome
Congenital imperforate anus
Lobster-claw hand
Blepharophimosis, intellectual disability syndrome/genitopatellar overlap syndrome
Genitourinary congenital anomalies
WAGR (Wilms tumour, aniridia, genitourinary anomalies and mental retardation) syndrome
Autosomal recessive faciodigitogenital syndrome
Harrod syndrome
Aarskog-like syndrome
Intellectual disability and short stature with hand contracture and genital anomaly syndrome
Intrauterine growth restriction, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomaly syndrome
Pfeiffer Kapferer syndrome
Craniofacial digital and genital anomalies syndrome
Wilms tumour, aniridia, genitourinary anomalies and mental retardation syndrome
Dysmorphism, short stature, deafness, pseudohermaphroditism syndrome
Wilms tumor, aniridia, genitourinary anomalies and mental retardation syndrome
Lethal hemolytic anemia and genital anomaly syndrome
Johnson Munson syndrome
Prader Willi habitus with osteopenia and camptodactyly
Anal atresia
Congenital malformation of genital organs
Cranio-facio-digito-genital syndrome
PELVIS syndrome
Proud syndrome
Perineal haemangioma, external genitalia malformation, lipomyelomeningocele, vesicorenal abnormality, imperforate anus syndrome

Frequently Asked Questions

What is the ICD-10 code for congenital malformation of male genital organ, unspecified?

The ICD-10-CM code for congenital malformation of male genital organ, unspecified is Q55.9. The full clinical description is "Congenital malformation of male genital organ, unspecified". Q55.9 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code Q55.9 mean?

ICD-10-CM code Q55.9 represents “Congenital malformation of male genital organ, unspecified”. 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 Q55.9 a billable code?

Yes, Q55.9 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is Q55.9 in?

Q55.9 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).

What codes cannot be used with Q55.9?

Q55.9 has Excludes1 notes indicating codes that cannot be used together with it, including: androgen insensitivity syndrome (E34.5-); syndromes associated with anomalies in the number and form of chromosomes (Q90-Q99); congenital hydrocele (P83.5); and 1 more.

What SNOMED CT codes does Q55.9 map to?

Q55.9 maps to 48 SNOMED CT concepts: 4135001, 880094008, 879938005, 1231281009, 890221004, and 43 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for Q55.9?

Q55.9 is linked to 2 UMLS Concept Unique Identifiers: C2910222, C0266421. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does Q55.9 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like congenital malformation of male genital organ, unspecified 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 Q55.9?

Q55.9 maps to the ICD-11 code: LB5Z (Structural developmental anomalies of the male genital system, 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.