Pages that link to "Property:P89"
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The following pages link to Linked ICD 10 (P89):
Displaying 50 items.
- Keratinopathic ichthyoses (Q46657) (← links)
- Autosomal recessive congenital ichthyosis (Q46658) (← links)
- Hidrotic ectodermal dysplasia, Clouston type (Q46659) (← links)
- Pseudoxanthoma elasticum (Q46660) (← links)
- Papular palmoplantar keratodermas (Q46661) (← links)
- Non-syndromic ichthyosis (Q46662) (← links)
- Genetic disorders of skin pigmentation (Q46663) (← links)
- Breast aplasia (Q46664) (← links)
- Supernumerary breasts (Q46665) (← links)
- Absent nipple (Q46666) (← links)
- Accessory nipple (Q46667) (← links)
- Genetic syndromes with alopecia or hypotrichosis (Q46668) (← links)
- Genetic defects of the hair shaft (Q46669) (← links)
- Genetic syndromes with hypertrichosis (Q46670) (← links)
- Developmental defects of hair or hair growth (Q46671) (← links)
- Genetic syndromes with abnormalities of the hair shaft (Q46672) (← links)
- Genetic defects of hair or hair growth (Q46673) (← links)
- Genetic defects of nails or nail growth (Q46674) (← links)
- Genetic syndromes affecting nails (Q46675) (← links)
- Developmental defects of the nail apparatus (Q46676) (← links)
- Inherited deformities of nails (Q46677) (← links)
- Aplasia cutis congenita (Q46678) (← links)
- Dermoid cyst (Q46679) (← links)
- Neurofibromatosis type 2 (Q46680) (← links)
- Gardner syndrome (Q46681) (← links)
- Neurofibromatoses (Q46682) (← links)
- Neurofibromatosis type 3 (Q46683) (← links)
- Phakomatoses or hamartoneoplastic syndromes (Q46684) (← links)
- Gorlin syndrome (Q46685) (← links)
- Peutz-Jeghers syndrome (Q46686) (← links)
- Neurofibromatosis type 1 (Q46687) (← links)
- Tuberous sclerosis (Q46688) (← links)
- Connective tissue hamartoma (Q46689) (← links)
- Pilosebaceous hamartoma (Q46690) (← links)
- Complex epidermal hamartoma (Q46691) (← links)
- Keratinocytic epidermal hamartoma (Q46692) (← links)
- Fetal Valproate Spectrum Disorder (Q46693) (← links)
- Toxic or drug-related embryofetopathies (Q46694) (← links)
- Fetal alcohol syndrome (Q46695) (← links)
- Fetal hydantoin syndrome (Q46696) (← links)
- Embryofetopathy due to oral anticoagulant therapy (Q46697) (← links)
- Genetic hamartoneoplastic syndromes affecting the skin (Q46698) (← links)
- Pierre Robin syndrome (Q46699) (← links)
- Prader-Willi syndrome (Q46700) (← links)
- Noonan syndrome (Q46701) (← links)
- Constriction rings (Q46702) (← links)
- VATER association (Q46703) (← links)
- Syndromes with limb duplication, polydactyly, syndactyly or triphalangism (Q46704) (← links)
- Complex brachydactylies (Q46705) (← links)
- Congenital vascular bone syndromes (Q46706) (← links)
