Pediatrics conditions, page 3 of 3
9 conditions on this page, alphabetically from Neonatal abstinence syndrome to Zika virus congenital syndrome. Each entry below describes the condition in full.
On this page
Neonatal abstinence syndrome
A withdrawal disorder that is characterized by a group of problems that occur in a newborn who was exposed to addictive illegal or prescription drugs while in the mother's womb or postnatally following the discontinuance of drug treatment. Our Pediatrics team evaluates and manages neonatal abstinence syndrome.
Also known as
- Drug withdrawal syndrome in newborn
Classification
Ontology identifier: DOID:9828 (Human Disease Ontology).
Classification path: disease of mental health › substance-related disorder › withdrawal disorder.
Specialty: Pediatrics
Broader conditions
Medical codes
- ICD-10-CM: P96.1
- ICD-9-CM: 779.5
- MeSH: D009357
- SNOMED CT: 414819007
Care at Weyland-Yutani Health System
At Weyland-Yutani Health System, neonatal abstinence syndrome is managed by Pediatrics with support from imaging, laboratory and rehabilitation services where needed.
Treatment options
Diagnostic tests
Related articles
When to seek care
If you or a family member may have neonatal abstinence syndrome, contact your primary care provider or schedule a visit with Pediatrics.
Reference links
Neonatal diabetes mellitus
Overview. A diabetes mellitus that is characterized by hyperglycemia occurring within the first 6 months of life. Weyland-Yutani Health System offers diagnosis and ongoing care for neonatal diabetes mellitus.
Also known as
- diabetes mellitus syndrome in newborn infant
- neonatal diabetes
Classification
Ontology identifier: DOID:11717 (Human Disease Ontology).
Classification path: disease of metabolism › inherited metabolic disorder › carbohydrate metabolic disorder › glucose metabolism disease › diabetes mellitus.
Specialty: Pediatrics
Broader conditions
Medical codes
- ICD-10-CM: P70.2
- ICD-9-CM: 775.1
- SNOMED CT: 49817004
Care at Weyland-Yutani Health System
At Weyland-Yutani Health System, neonatal diabetes mellitus is managed by Pediatrics with support from imaging, laboratory and rehabilitation services where needed.
Treatment options
Diagnostic tests
Related articles
When to seek care
Seek a medical evaluation if you are concerned about neonatal diabetes mellitus. Bring a list of current medications and any previous test results.
Reference links
Neonatal jaundice
Overview. A pigmentation disease characterized by a high level of bilirubin in the blood, causing a yellowing of the skin and other tissues of a newborn infant. Weyland-Yutani Health System offers diagnosis and ongoing care for neonatal jaundice.
Also known as
- neonatal hyperbilirubinemia
- neonatal icterus
Classification
Ontology identifier: DOID:2383 (Human Disease Ontology).
Classification path: disease of anatomical entity › integumentary system disease › skin disease › pigmentation disease.
Specialty: Pediatrics
Broader conditions
Medical codes
- ICD-10-CM: P59.9
- MeSH: D007567
- SNOMED CT: 299968002
Care at Weyland-Yutani Health System
Treatment of neonatal jaundice begins with an evaluation in Pediatrics. Follow-up visits track how you are responding to care.
Treatment options
Diagnostic tests
Related articles
When to seek care
If you or a family member may have neonatal jaundice, contact your primary care provider or schedule a visit with Pediatrics.
Reference links
Omphalocele
Overview. A physical disorder characterized by a defect in the development of the abdominal wall muscles, resulting in the intestines, liver and other organs to remain outside of the abdomen in a sac. Weyland-Yutani Health System offers diagnosis and ongoing care for omphalocele.
Also known as
Classification
Ontology identifier: DOID:0060327 (Human Disease Ontology).
Classification path: physical disorder.
Specialty: Pediatrics
Medical codes
- ICD-10-CM: Q79.2
- ICD-9-CM: 756.72
- MeSH: D000099245
- OMIM: 164750
- SNOMED CT: 49324006
- SNOMED CT: 5867007
Care at Weyland-Yutani Health System
Pediatrics specialists lead care for omphalocele. Plans are tailored to each patient and reviewed regularly.
Treatment options
Diagnostic tests
When to seek care
Questions about omphalocele? Call your nearest Weyland-Yutani location and ask for Pediatrics.
Reference links
Poland syndrome
Overview. A physical disorder that is characterized by missing or underdeveloped muscles on one side of the body, resulting in abnormalities that can affect the chest, shoulder, arm, and hand. Weyland-Yutani Health System offers diagnosis and ongoing care for Poland syndrome.
Also known as
- Poland anomaly
- Poland's syndactyly
Classification
Ontology identifier: DOID:12961 (Human Disease Ontology).
Classification path: physical disorder.
Specialty: Pediatrics
Medical codes
- ICD-10-CM: Q79.8
- MeSH: D011045
- OMIM: 173800
- SNOMED CT: 205524002
Care at Weyland-Yutani Health System
Care for Poland syndrome is coordinated through Pediatrics. Your clinician will recommend tests and treatments based on your history and symptoms.
Treatment options
Diagnostic tests
Related articles
When to seek care
Questions about Poland syndrome? Call your nearest Weyland-Yutani location and ask for Pediatrics.
Reference links
Severe congenital encephalopathy due to MECP2 mutation
A brain disease characterized by severe neonatal encephalopathy, developmental delay, and microcephaly that has_material_basis_in hemizygous mutation in the MECP2 gene on chromosome Xq28. Patients with severe congenital encephalopathy due to MECP2 mutation are cared for through our Pediatrics service line.
Also known as
- neonatal severe encephalopathy due to MECP2 mutations
- severe neonatal-onset encephalopathy with microcephaly
Classification
Ontology identifier: DOID:0111932 (Human Disease Ontology).
Classification path: genetic disease › monogenic disease › X-linked monogenic disease › X-linked recessive disease.
Specialty: Pediatrics
Broader conditions
Medical codes
- MeSH: C566878
- OMIM: 300673
- SNOMED CT: 711487002
Care at Weyland-Yutani Health System
At Weyland-Yutani Health System, severe congenital encephalopathy due to MECP2 mutation is managed by Pediatrics with support from imaging, laboratory and rehabilitation services where needed.
Treatment options
Diagnostic tests
When to seek care
Questions about severe congenital encephalopathy due to MECP2 mutation? Call your nearest Weyland-Yutani location and ask for Pediatrics.
Reference links
Spina bifida
A neural tube defect that is characterized by incomplete closing of the spine and membranes around the spinal cord during early development. Patients with spina bifida are cared for through our Pediatrics service line.
Classification
Ontology identifier: DOID:0080016 (Human Disease Ontology).
Classification path: physical disorder › neural tube defect.
Specialty: Pediatrics
More specific conditions
Medical codes
- ICD-10-CM: Q05
- ICD-9-CM: 741
- MeSH: D016135
- SNOMED CT: 156888006
Care at Weyland-Yutani Health System
Pediatrics specialists lead care for spina bifida. Plans are tailored to each patient and reviewed regularly.
Treatment options
Diagnostic tests
Related articles
When to seek care
If you or a family member may have spina bifida, contact your primary care provider or schedule a visit with Pediatrics.
Reference links
Systemic juvenile rheumatoid arthritis
Overview. A rheumatoid arthritis that involves an autoimmune disease onset in children under 16 which attacks the healthy cells and tissue of located_in joint. Weyland-Yutani Health System offers diagnosis and ongoing care for systemic juvenile rheumatoid arthritis.
Also known as
- acute juvenile rheumatoid arthritis
- juvenile chronic polyarthritis
- juvenile idiopathic arthritis
- juvenile rheumatoid arthritis
- monarticular juvenile rheumatoid arthritis
- pauciarticular juvenile arthritis
- Pauciarticular onset juvenile chronic arthritis
- Still's disease
Classification
Ontology identifier: DOID:676 (Human Disease Ontology).
Classification path: disease of anatomical entity › immune system disease › primary immunodeficiency disease › rheumatoid arthritis.
Specialty: Pediatrics
Broader conditions
Medical codes
- ICD-10-CM: M08.4
- ICD-9-CM: 714.3
- ICD-9-CM: 714.31
- ICD-9-CM: 714.32
- ICD-9-CM: 714.33
- OMIM: 604302
- SNOMED CT: 201798003
- SNOMED CT: 74391003
- SNOMED CT: 7441009
- SNOMED CT: 83793004
Care at Weyland-Yutani Health System
Treatment of systemic juvenile rheumatoid arthritis begins with an evaluation in Pediatrics. Follow-up visits track how you are responding to care.
Treatment options
Diagnostic tests
When to seek care
If you or a family member may have systemic juvenile rheumatoid arthritis, contact your primary care provider or schedule a visit with Pediatrics.
Reference links
Zika virus congenital syndrome
A syndrome that is characterized in neonates by microcephaly, craniofacial disproportion, spasticity, seizures, irritability and brainstem dysfunction including feeding difficulties, ocular abnormalities and findings on neuroimaging such as calcifications, cortical disorders and ventriculomegaly and has_material_basis_in the acquisition of Zika virus (Orthoflavivirus zikaense) infection in utero. Our Pediatrics team evaluates and manages Zika virus congenital syndrome.
Also known as
- congenital Zika syndrome
- ZIKV congenital infection
Classification
Ontology identifier: DOID:0080180 (Human Disease Ontology).
Classification path: physical disorder.
Specialty: Pediatrics
Broader conditions
Medical codes
- MeSH: D000071243
- SNOMED CT: 762725007
Care at Weyland-Yutani Health System
Pediatrics specialists lead care for Zika virus congenital syndrome. Plans are tailored to each patient and reviewed regularly.
Treatment options
Diagnostic tests
When to seek care
Seek a medical evaluation if you are concerned about Zika virus congenital syndrome. Bring a list of current medications and any previous test results.
Reference links