Q55.9
BillableCongenital malformation of male genital organ, unspecified
Congenital malformation of male genital organ, unspecified
Status
Billable / Specific
Parent Code
Q55Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Congenital anomaly of male genital organ
- Congenital deformity of male genital organ
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
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
- 11p partial monosomy syndrome4135001
- Congenital anomaly of male genital system4406004
- Congenital cleft hand13624003
- Lobster claw hand13624003
- Lobster-claw hand13624003
- Arachnodactyly62250003
- Congenital arachnodactyly62250003
- Spider finger62250003
- Centronuclear myopathy82077006
- Myotubular myopathy82077006
- Congenital absence of radius84918006
- Frontonasal dysplasia sequence86610004
- Median cleft face syndrome86610004
- CAH - Congenital adrenal hypoplasia93235007
- Congenital adrenal hypoplasia93235007
- Congenital hypoplasia of adrenal gland93235007
- Congenital small adrenal gland93235007
- Anal atresia204712000
- Aproctia204712000
- Atresia ani204712000
- Congenital atresia of anus204712000
- Congenital imperforate anus204712000
- Imperforate anus204712000
- Congenital anomaly of genital organ204821009
- Congenital deformity of genital organ204821009
- Congenital genital organ anomalies204821009
- Congenital malformation of genital organs204821009
- Congenital obstructive azoospermia236807008
- Telecanthus246803005
- Congenital urogenital anomaly287085006
- Genitourinary congenital anomalies287085006
- Congenital anomaly of male urogenital tract428522008
- Congenital male urogenital anomaly428522008
- Genitopatellar syndrome702367005
- IMAGe syndrome702384004
- Intrauterine growth restriction, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomaly syndrome702384004
- Hydrometrocolpos, postaxial polydactyly, and congenital heart malformation702407009
- McKusick Kaufman syndrome702407009
- Hand-foot-genital syndrome702425002
- Hand-foot-uterus syndrome702425002
- Chromosome 11p13 deletion syndrome715215007
- WAGR (Wilms tumor, aniridia, genitourinary anomalies and mental retardation) syndrome715215007
- WAGR (Wilms tumour, aniridia, genitourinary anomalies and mental retardation) syndrome715215007
- WAGR syndrome715215007
- Wilms tumor, aniridia, genitourinary anomalies and mental retardation syndrome715215007
- Wilms tumour, aniridia, genitourinary anomalies and mental retardation syndrome715215007
- Cranio-facio-digito-genital syndrome716089008
- Craniofacial digital and genital anomalies syndrome716089008
- Harrod syndrome716089008
- Intellectual disability and short stature with hand contracture and genital anomaly syndrome716334004
- Prader Willi habitus with osteopenia and camptodactyly716334004
- Urban Rogers Meyer syndrome716334004
- X-linked lissencephaly with abnormal genitalia syndrome717632002
- X-linked lissencephaly with agenesis of corpus callosum and genital anomaly syndrome717632002
- X-linked lissencephaly with ambiguous genitalia717632002
- Lethal haemolytic anaemia and genital anomaly syndrome719402008
- Lethal hemolytic anemia and genital anomaly syndrome719402008
- Waters West syndrome719402008
- Disorder of sex development with intellectual disability syndrome719450007
- Pseudohermaphroditism with intellectual disability syndrome719450007
- Verloes Gillerot Fryns syndrome719450007
- Deafness, genital anomaly, metacarpal and metatarsal synostosis syndrome721086004
- Pfeiffer Kapferer syndrome721086004
- STAR (syndactyly, telecanthus, anogenital, renal malformation) syndrome723581006
- STAR syndrome723581006
- Syndactyly, telecanthus, anogenital and renal malformation syndrome723581006
- Casamassima Morton Nance syndrome723610009
- Spondylocostal dysostosis with anal atresia and genitourinary malformation syndrome723610009
- ALX4 (human aristaless-like 4) related frontonasal dysplasia with alopecia and genital anomaly725029001
- Craniofrontonasal dysplasia with alopecia and hypogonadism725029001
- Frontonasal dysplasia with alopecia and genital abnomality725029001
- Frontonasal dysplasia with alopecia and genital anomaly syndrome725029001
- PELVIS (Perineal haemangioma, external genitalia malformation, lipomyelomeningocele, vesicorenal abnormality, imperforate anus) syndrome725138002
- PELVIS (perineal hemangioma, external genitalia malformation, lipomyelomeningocele, vesicorenal abnormality, imperforate anus) syndrome725138002
- PELVIS syndrome725138002
- Perineal haemangioma, external genitalia malformation, lipomyelomeningocele, vesicorenal abnormality, imperforate anus syndrome725138002
- Perineal hemangioma, external genitalia malformation, lipomyelomeningocele, vesicorenal abnormality, imperforate anus syndrome725138002
- Aarskog-like syndrome725434009
- Autosomal recessive facio-digito-genital syndrome725434009
- Autosomal recessive faciodigitogenital syndrome725434009
- Facio-digito-genital syndrome Kuwait type725434009
- Teebi Naguib Alawadi syndrome725434009
- Deletion of part of chromosome 11726381002
- Dysmorphism, short stature, deafness, disorder of sex development syndrome733050004
- Dysmorphism, short stature, deafness, pseudohermaphroditism syndrome733050004
- Aphalangy, hemivertebra, urogenital, intestinal dysgenesis syndrome733118006
- Johnson Munson syndrome733118006
- Agenesis of corpus callosum and abnormal genitalia syndrome763797003
- Corpus callosum agenesis, abnormal genitalia syndrome763797003
- Microcephaly, corpus callosum agenesis, abnormal genitalia syndrome763797003
- Proud Levine Carpenter syndrome763797003
- Proud syndrome763797003
- Absent radius, anogenital anomalies syndrome771264005
- RAB18 deficiency772225005
- RAB18, member RAS oncogene family deficiency772225005
- 46,XY disorder of sex development due to environmental chemical exposure879938005
- 46,XY disorder of sex development880094008
- ACFS - acrocardiofacial syndrome890221004
- Acro-cardio-facial syndrome890221004
- Acrocardiofacial syndrome890221004
- CCGE - cleft palate, cardiac defect, genital anomalies, ectrodactyly syndrome890221004
- Cleft palate, cardiac defect, genital anomalies, and ectrodactyly890221004
- Aplasia of bone of forearm1145452004
- Aplasia of bone of radius and/or ulna1145452004
- Aplasia of radius1145466009
- Agammaglobulinaemia due to TOP2B mutation1230295000
- Agammaglobulinemia due to TOP2B mutation1230295000
- B-cell immunodeficiency, limb anomaly, urogenital malformation syndrome1230295000
- BILU (B-cell immunodeficiency, limb, urogenital) syndrome1230295000
- BILU syndrome1230295000
- Hoffman syndrome due to TOP2B deficiency1230295000
- 46,XY disorder of sex development due to isolated 17,20-lyase deficiency1231281009
- MIRAGE (myelodysplasia, infection, restriction of growth, adrenal hypoplasia, genital anomalies, enteropathy) syndrome1234831009
- MIRAGE syndrome1234831009
- Myelodysplasia, infection, restriction of growth, adrenal hypoplasia, genital anomalies, enteropathy syndrome1234831009
- Myelodysplasia, infection, restriction of growth, adrenal hypoplasia, genital phenotypes, enteropathy syndrome1234831009
- X-linked myotubular myopathy, abnormal genitalia syndrome1255278004
- Xq28 contiguous gene deletion syndrome1255278004
- Blepharophimosis, intellectual disability syndrome/genitopatellar overlap syndrome1304113005
- Cardiac urogenital syndrome1332387008
- MYRF-related cardiac urogenital syndrome1332387008
- Myelin regulatory factor-related cardiac urogenital syndrome1332387008
- Short stature co-occurrent and due to endocrine disorder368331000119100
UMLS
- Congenital anomaly of male genital organC2910222
- Congenital anomaly of male genital systemC0266421
- Congenital anomaly of male genital system (disorder)C0266421
- Congenital deformity of male genital organC0266421
- Congenital genital malformation maleC0266421
- Congenital malformation of male genital organ, unspecifiedC0266421
- Other congenital malformations of male genital organsC0266421
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.
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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.