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ICD-10-CM Code for Congenital adrenogenital disorders associated with enzyme deficiency E25.0

ICD-10 code E25.0 for Congenital adrenogenital disorders associated with enzyme deficiency is a medical classification as listed by WHO under the range - Endocrine, nutritional and metabolic diseases .

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Official Long Descriptor

Congenital adrenogenital disorders associated with enzyme deficiency
Congenital adrenal hyperplasia
21-Hydroxylase deficiency
Salt-losing congenital adrenal hyperplasia

E25

Includes: adrenogenital syndromes, virilizing or feminizing, whether acquired or due to adrenal hyperplasia consequent on inborn enzyme defects in hormone synthesis
Female adrenal pseudohermaphroditism
Female heterosexual precocious pseudopuberty
Male isosexual precocious pseudopuberty
Male macrogenitosomia praecox
Male sexual precocity with adrenal hyperplasia
Male virilization (female)

Excludes1: indeterminate sex and pseudohermaphroditism (Q56)
chromosomal abnormalities (Q90-Q99)

Additional/Related Information

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Get crucial instructions for accurate ICD-10-CM E25.0 coding with all applicable Excludes 1 and Excludes 2 notes from the section level conveniently shown with each code.
This section shows you chapter-specific coding guidelines to increase your understanding and correct usage of the target ICD-10-CM Volume 1 code.

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ICD-10 Mutually Exclusive
[QUOTE="mitchellde, post: 445232, member: 30657"]for the example you gave E78.00 with E29.1 the edit for mutually exclusive diagnosis is correct. look under the subsection Metabolic disorders (E70-... [ Read More ]
ICD-10 Mutually Exclusive
for the example you gave E78.00 with E29.1 the edit for mutually exclusive diagnosis is correct. look under the subsection Metabolic disorders (E70-E88) Type 1 Excludes: •androgen insensitivi... [ Read More ]
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