ICD 9 Angelman Syndrome-Wiki Finder
ICD 9 Angelman Syndrome

ICD 9 Angelman Syndrome


Angelman syndrome - Wikipedia, the free encyclopedia

Angelman syndrome (abbreviated AS) is a neuro- genetic disorder characterized by severe intellectual and developmental disability, sleep disturbance, seizures, jerky ...


List of ICD-9 codes 740–759: congenital anomalies ...

14. Congenital anomalies (740–759) Nervous system (740-742) Anencephalus and similar anomalies Anencephalus; Spina bifida Other congenital anomalies of nervous system


Orphanet: Angelman syndrome

Summary. Angelman syndrome (AS) is a neurogenetic disorder characterized by severe intellectual deficit and distinct facial dysmorphic features.


Frequently Asked Questions About Angelman Syndrome ...

FASTFAQs Frequently Asked Questions About Angelman Syndrome What Does This Mean, and Why Does This Matter? An important question that may arise with the …


2015 ICD-10-CM Alpha Index > 'S' Terms > Syndrome - Page 1/7

Toggle navigation. ICD-10-CM Codes; ICD-10-CM Indexes; Conversion; Coding Rules ... 2015 ICD-10-CM Alpha Index > 'S' Terms >

From:http://www.icd10data.com › 2015 ICD-10-CM Alpha Index › 'S'

Famous People with Angelman Syndrome | HRF

In 2007, October he was so sad to know that his son James is suffering from a health condition called Angelman Syndrome. It really breaks the heart of the actor.

From:http://healthresearchfunding.org › Medical Articles and Infographics

2015 ICD-10-CM Alpha Index > Starting with 'A' (702)

ICD-10-CM Alpha Index > Starting with 'A' (702) > Aarskog's syndrome Q87.1; Abandonment - see Maltreatment; Abasia (-astasia) (hysterical) F44.4

From:http://www.icd10data.com › ICD-10-CM Alpha Index

ICD-9-CM Diagnostic Codes for persons with related conditions

Center for Policy and Innovation Page 3 of 18 April 1, 2014 Specific Delays in Development (315.9) 315.9 Unspecified delay in development (developmental disorder …


Sindrome di Angelman - Wikipedia

La sindrome di Angelman è una malattia genetica dovuta a un difetto nella duplicazione cromosomica da imprinting genetico . Indice 1 Cenni storici 2 Patologie ...


short stature | Hereditary Ocular Diseases

This is a rare congenital disorder with so far incomplete phenotypic delineation. The diagnosis can be made soon after birth from the general facial and body morphology.



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