P94.2
BillableCongenital hypotonia
Congenital hypotonia
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Floppy baby syndrome, unspecified
Includes
Conditions included under this code
- conditions that have their origin in the fetal or perinatal period (before birth through the first 28 days after birth) even if morbidity occurs later
Excludes 2
Conditions not included here, but the patient may have both
Also Known As / Clinical Terms
SNOMED CT
- Flaccid newborn34761004
- Limp newborn34761004
- Cystinuria, type 137183000
- Recessive cystinuria37183000
- CSNU - Cystinuria85020001
- Cystinuria85020001
- Congenital hypoplasia of ulna93300007
- Congenital short ulna93300007
- Floppy baby205294008
- Floppy infant205294008
- Floppy infant syndrome205294008
- Neonatal hypotonia205294008
- Benign congenital hypotonia240080003
- Respiratory insufficiency syndrome of newborn276536005
- Neonatal neuromuscular disorder363222009
- Left ventricular myocardial noncompaction cardiomyopathy447935001
- Ventricular myocardial noncompaction cardiomyopathy471875005
- Hypertrophic mitochondrial cardiomyopathy472316006
- Hypertrophic cardiomyopathy with hypotonia and lactic acidosis syndrome718713000
- Dysharmonic skeletal maturation and muscular fiber disproportion syndrome721887007
- Dysharmonic skeletal maturation and muscular fibre disproportion syndrome721887007
- Puerto Rican infant hypotonia syndrome721887007
- Qazi Markouizos syndrome721887007
- Hypotonia, speech impairment, severe cognitive delay syndrome763722004
- IHPRF (infantile hypotonia, psychomotor retardation, characteristic facies) syndrome763722004
- Congenital disorder of glycosylation due to PIGT (phosphatidylinositol glycan anchor biosynthesis class T) deficiency770755007
- Congenital disorder of glycosylation due to PIGT deficiency770755007
- Intellectual disability, seizures, hypotonia, ophthalmologic, skeletal anomalies syndrome770755007
- MCAHS (multiple congenital anomalies, hypotonia, seizures syndrome) type 3770755007
- Congenital cataract, progressive muscular hypotonia, deafness, developmental delay syndrome773398005
- Congenital cataract, progressive muscular hypotonia, hearing loss, developmental delay syndrome773398005
- Short ulna, dysmorphism, hypotonia, intellectual disability syndrome773556006
- Intellectual disability, hypotonia, brachycephaly, pyloric stenosis, cryptorchidism syndrome773621003
- MCAHS (multiple congenital anomalies, hypotonia, seizures syndrome) type 2773643006
- Multiple congenital anomalies, hypotonia, seizures syndrome type 2773643006
- Growth and developmental delay, hypotonia, vision impairment, lactic acidosis syndrome774205007
- Atypical hypotonia cystinuria syndrome778025006
- Congenital disorder of glycosylation due to PIGN (phosphatidylinositol glycan anchor biosynthesis class N) deficiency785303004
- Multiple congenital anomalies, hypotonia, seizures syndrome785303004
- PIGN-CDG - phosphatidylinositol glycan anchor biosynthesis class N congenital disorder of glycosylation785303004
- Congenital hypoplasia of bone of forearm1145430008
- Congenital hypoplasia of bone of radius and/or ulna1145430008
- Lethal left ventricular non-compaction, seizures, hypotonia, cataract, developmental delay syndrome1172839002
- Postnatal microcephaly, infantile hypotonia, spastic diplegia, dysarthria, intellectual disability syndrome1173998003
- Severe hypotonia, psychomotor developmental delay, strabismus, cardiac septal defect syndrome1187212004
- Severe intellectual disability, hypotonia, strabismus, coarse face, planovalgus syndrome1197591008
- Baker Gordon syndrome1217371005
- Infantile hypotonia, oculomotor anomalies, hyperkinetic movements, developmental delay syndrome1217371005
- SYT1-related neurodevelopmental disorder1217371005
- Synaptotagmin 1-related neurodevelopmental disorder1217371005
- CLIFAHDD (congenital limbs, face contractures, hypotonia, developmental delay) syndrome1255322002
- CLIFAHDD syndrome1255322002
- Congenital contracture of limbs and face, hypotonia, developmental delay syndrome1255322002
- Fatal pontocerebellar hypoplasia, hypotonia, respiratory distress syndrome1362022003
- Fatal pontocerebellar hypoplasia, hypotonia, respiratory insufficiency syndrome1362022003
- Lethal pontocerebellar hypoplasia, hypotonia, respiratory insufficiency syndrome1362022003
UMLS
- floppy babyC0270971
- floppy infantC0270971
- Congenital floppy infantC0270971
- Congenital hypotoniaC0270971
- Floppy InfantC0270971
- Floppy Infant SyndromeC0270971
- Floppy babyC0270971
- Floppy baby syndrome, unspecifiedC0270971
- Floppy infantC0270971
- Floppy infant syndromeC0270971
- Hypotonia, congenitalC0270971
- Infantile HypotoniaC0270971
- babies floppyC0270971
- congenital hypotoniaC0270971
- floppy infant syndromeC0270971
- floppy infantsC0270971
- hypotonia congenitalC0270971
- infant floppyC0270971
- neonatal hypotoniaC0270971
Frequently Asked Questions
What is the ICD-10 code for congenital hypotonia?
The ICD-10-CM code for congenital hypotonia is P94.2. The full clinical description is "Congenital hypotonia". P94.2 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code P94.2 mean?
ICD-10-CM code P94.2 represents "Congenital hypotonia". It is classified under Chapter 16: Certain Conditions Originating in the Perinatal Period and is a billable/specific code that can be used on a claim.
Is P94.2 a billable code?
Yes, P94.2 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is P94.2 in?
P94.2 is in Chapter 16: Certain Conditions Originating in the Perinatal Period (codes P00-P96).
What SNOMED CT codes does P94.2 map to?
P94.2 maps to 30 SNOMED CT concepts: 778025006, 1217371005, 240080003, 1255322002, 85020001, and 25 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for P94.2?
P94.2 is linked to 1 UMLS Concept Unique Identifier: C0270971. 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.