ICD-10: Z82.7
Family history of congenital malformations, deformations and chromosomal abnormalities
Clinical Information
Inclusion Terms
- Conditions classifiable to Q00-Q99
Subcategories
Related Diseases
fragile X-associated tremor/ataxia syndrome
cerebellar ataxia, mental retardation and dysequlibrium syndrome
Pearson syndrome
childhood spinal muscular atrophy
Stormorken syndrome
Vici syndrome
Galloway-Mowat syndrome 1
orofaciodigital syndrome IV
chondrodysplasia Blomstrand type
chromosome 16q22 deletion syndrome
Warsaw breakage syndrome
Ritscher-Schinzel syndrome
syndromic X-linked intellectual disability 5
syndromic X-linked intellectual disability 17
Miles-Carpenter syndrome
syndromic X-linked intellectual disability Chudley-Schwartz type
Christianson syndrome
Griscelli syndrome type 2
autosomal recessive pseudohypoaldosteronism type 1
autosomal dominant pseudohypoaldosteronism type 1
Kartagener syndrome
Frasier syndrome
Charcot-Marie-Tooth disease type X
obsolete Saldino-Noonan syndrome
glycogen storage disease XV
acrokeratosis verruciformis
Aland Island eye disease
anauxetic dysplasia 1
obsolete anonychia congenita
Baller-Gerold syndrome
Bamforth-Lazarus syndrome
blue cone monochromacy
COX deficiency, infantile mitochondrial myopathy
tyrosinemia type III
congenital intrinsic factor deficiency
Qazi Markouizos syndrome
spastic ataxia 1
cerebral creatine deficiency syndrome
Perrault syndrome
obsolete CLONE OF congenital afibrinogenemia
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