E03.1 CONGENITAL HYPOTHYROIDISM WITHOUT GOITER

Synonyms

• Brain lung thyroid syndrome
• Central hypothyroidism
• Central hypothyroidism
• Central hypothyroidism
• Choanal atresia
• Choanal atresia, athelia, hypothyroidism, delayed puberty, short stature syndrome
• Congenital abnormality of nipple
• Congenital absence of thyroid gland
• Congenital atresia of nasopharynx
• Congenital atresia of pharynx
• Congenital atrophy of thyroid
• Congenital central hypothyroidism
• Congenital central hypothyroidism due to thyrotropin-releasing hormone receptor deficiency
• Congenital hypothyroidism
• Congenital hypothyroidism due to absence of thyroid gland
• Congenital hypothyroidism due to congenital anomaly of thyroid gland
• Congenital hypothyroidism due to dual oxidase maturation factor 2
• Congenital hypothyroidism due to maternal intake of antithyroid drug
• Congenital hypothyroidism due to peripheral resistance to thyroid hormone
• Congenital hypothyroidism due to symporter mutation
• Congenital hypothyroidism due to thyroglobulin mutation
• Congenital hypothyroidism due to thyroid deiodinase mutation
• Congenital hypothyroidism due to thyroid peroxidase mutation
• Congenital hypothyroidism due to thyroid stimulating hormone receptor mutation
• Congenital hypothyroidism due to transplacental passage of maternal thyroid stimulating hormone binding inhibitory antibody
• Congenital hypothyroidism without goiter
• Congenital iodine deficiency syndrome
• Congenital thyroid hypoplasia
• Developmental malformation of branchial arch
• Ear, face and neck congenital anomalies
• Familial thyroid dyshormonogenesis
• Genetic transient congenital hypothyroidism
• Hypertrophy of testis
• Hypoplasia of thyroid
• Hypothyroidism due to mutation in transcription factor of pituitary development
• Idiopathic congenital hypothyroidism
• Infant hypothyroidism
• Neonatal diabetes, congenital hypothyroidism, congenital glaucoma, hepatic fibrosis, polycystic kidney syndrome
• Neonatal jaundice with congenital hypothyroidism
• Obesity, colitis, hypothyroidism, cardiac hypertrophy, developmental delay syndrome
• Primary hypothyroidism
• Primary hypothyroidism
• Primary hypothyroidism
• Resistance to thyroid hormone due to mutation in thyroid hormone receptor alpha
• Thyroid atrophy
• Thyroid degeneration
• Thyroid hemiagenesis
• Transient congenital hypothyroidism due to dual oxidase 2 mutation
• Transient hypothyroidism
• Transient hypothyroidism
• Transient hypothyroidism
• Transient hypothyroidism
• X-linked central congenital hypothyroidism with late-onset testicular enlargement

Diagnostic Related Group(s)

The code E03.1 is grouped in the following Diagnostic Related Group(s) MS-DRG V42.0

1. Endocrine Disorders With Mcc (643)
2. Endocrine Disorders With Cc (644)
3. Endocrine Disorders Without Cc/mcc (645)

References to Index of Diseases and Injuries

The code E03.1 has the following ICD-10-CM references to the Index of Diseases and Injuries

Crosswalk Information

ICD-10 Code		ICD-9 Code	ICD-9 Description
E03.1		243	Congenital hypothyroidsm

Similar Codes