# Congenital

<mark style="color:$danger;">**This Editorial Guide is used for Education Purposes Only. It is used in the Authoring Courses and Certifications. It is based on the January 2026 Editorial Guide.**</mark>

The concept 66091009 |Congenital disease (disorder)|, means present at birth. Though the word *congenital* may be applied to genetic disorders, the term *genetic* is preferred for those disorders.

The logical definition of a congenital disorder must include:

* Occurrence = Congenital (qualifier value).

It may also include:

* Finding site = X (body structure)
* Associated morphology = X (morphologic abnormality)
* Pathological process = Pathological development process (qualifier value)

All of these defining relationships should be grouped to indicate that the abnormal morphology occurs at the finding site, results from a pathological development process, and is present at birth. Where a morphologic abnormality occurs at more than one finding site, or one body structure has multiple morphologic abnormalities, multiple relationship groups should be created and the pathological process and occurrence relationships included in each relationship group.

The following guidelines apply:

A disorder with the word *congenital* in the FSN should classify under 66091009 |Congenital disease (disorder)|.

Congenital X (morphologic abnormality) concepts are being inactivated hence Congenital anomaly disorder grouper concepts, such as 9904008 |Congenital anomaly of cardiovascular system (disorder)|, should be modeled with an Associated morphology (attribute) of 49755003 |Morphologically abnormal structure (morphologic abnormality)I and a Pathological process relationship.

Whether creating new or revising existing concepts, only use Congenital X (morphologic abnormality) concepts if no non-congenital supertype of that morphologic abnormality is active.

* For example, use 399898009 |Misalignment (morphologic abnormality)| not 102283003 |Congenital misalignment (morphologic abnormality)|

{% hint style="warning" %}
**Neonatal period**

According to the American Medical Association, the periods of life in the *postnatal period* include all periods after birth including the neonatal or immediate postpartum period. It may be challenging to differentiate a congenital disorder from a neonatal disorder. A condition may be present at birth, i.e. congenital; however, clinical manifestations may take longer to appear, i.e. during the neonatal period (e.g. 14333004 |Alloimmune neonatal neutropenia (disorder)|).
{% endhint %}

When modeling a congenital neoplasm disorder, the attribute-value relationship of *Pathological process (attribute) = Pathological development process (qualifier value)* is not used.

## Congenital versus acquired

While some disorders are *only* congenital or *only* acquired, some disorders may be *either* congenital or acquired. The \_ acquired\_ form should only exist when there is a need to differentiate from the congenital form. Do not model a disorder as acquired if a congenital variant does not exist.

Congenital disorders are modeled using 246454002 |Occurrence (attribute)| of 255399007 |Congenital (qualifier value)|. If the FSN does not include *congenital* , it should not be modeled as congenital. The precise meaning of the FSN should be followed (e.g. many hereditary disorders have congenital appearances).

For example,

33534005 |Congenital bowing of femur (disorder)| is modeled with 246454002 |Occurrence (attribute)| of 255399007 |Congenital (qualifier value)|

<figure><img src="https://3063935683-files.gitbook.io/~/files/v0/b/gitbook-x-prod.appspot.com/o/spaces%2FSZh4aZdgpviXMYp37bCy%2Fuploads%2Fgit-blob-8d56b922105d6faebbb0f42c64c19577addd8af5%2Fimage%20(117).png?alt=media" alt=""><figcaption></figcaption></figure>

<figure><img src="https://github.com/SNOMED-Documents/snomed-editorial-guide/blob/main/authoring/clinical-finding-and-disorder/images/174690519.png" alt=""><figcaption><p>Stated view of 33534005 |Congenital bowing of femur (disorder)|</p></figcaption></figure>

Acquired disorders are those that originate and manifest after birth. The disorders are associated with a period of life, as opposed to a specific process or structure. All diseases (disorders) that occur after birth are considered *acquired*.

Generally, concepts that explicitly state *acquired* in the FSN or in a synonym should be modeled with Occurrence = 767023003 |Period of life beginning after birth and ending before death (qualifier value)|.

For example,

240253004 |Acquired abduction deformity of foot (disorder)| has *acquired* in the FSN and is modeled with Occurrence = 767023003 |Period of life beginning after birth and ending before death (qualifier value)|.

<figure><img src="https://3063935683-files.gitbook.io/~/files/v0/b/gitbook-x-prod.appspot.com/o/spaces%2FSZh4aZdgpviXMYp37bCy%2Fuploads%2Fgit-blob-ce7bd4027c2339855b5c9d57c9b459f378118b9c%2Fimage%20(118).png?alt=media" alt=""><figcaption></figcaption></figure>

<figure><img src="https://github.com/SNOMED-Documents/snomed-editorial-guide/blob/main/authoring/clinical-finding-and-disorder/images/174690518.png" alt=""><figcaption><p>Stated view of 240253004 |Acquired abduction deformity of foot (disorder)|</p></figcaption></figure>

{% hint style="info" %}
**Remodeling Acquired Disorders**

When revising acquired disorders, remove any acquired morphologies and replace with general parent morphologies, e.g. replace 127560004 |Acquired deformity (morphologic abnormality)| with 6081001 |Deformity (morphologic abnormality)|. Then add Occurrence attribute with a value of 767023003 | Period of life beginning after birth and ending before death (qualifier value)|. One of its children may also be used if the FSN states the period of life, such as *Childhood* or *Adulthood*.
{% endhint %}

## Congenital absence

Congenital absence can represent at least three different classes of absence:

1. Total developmental absence of the affected organ/structure
2. Partial absence of the affected organ/structure
3. In utero amputation of all or part of the affected organ/structure

Conventional use of the terms *aplasia* and *agenesis* often regard these as synonymous. However, proper definitions of these terms suggests a distinction that should be made in the terminology when included in the FSN.

* Aplasia - defective development resulting in the absence of all or part of an organ or tissue.
* Agenesis - absence of an organ due to nonappearance of its primordium in the embryo. (implies complete absence)

In order to conform to the intended meaning of the FSNs as described by the original source, the following modeling patterns are proposed for congenital absence terms:

Congenital absence of X

* Associated morphology = Absence (morphologic abnormality)
* Occurrence = Congenital (qualifier value)
* Finding site = Structure of X (body structure)
* Pathological process = Pathological developmental process (qualifier value)

Aplasia

* Associated morphology = Aplasia (morphologic abnormality)
* Occurrence = Congenital (qualifier value)
* Finding site = Structure of X (body structure)
* Pathological process = Pathological developmental process (qualifier value)

Partial absence of X

* Associated morphology = Aplasia (morphologic abnormality) or Transverse deficiency (morphologic abnormality)
* Occurrence = Congenital (qualifier value)
* Finding site = Part of X (body structure)
* Pathological process = Pathological developmental process (qualifier value)

Agenesis of X or Complete absence of X

* Associated morphology = Agenesis (morphologic abnormality)
* Occurrence = Congenital (qualifier value)
* Finding site = Entire X (body structure)
* Pathological process = Pathological developmental process (qualifier value)

#### *See also relative sections:*

* *Acquired abnormality of congenital anomaly*
* *Malformation, deformation, anomaly*

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