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From determinar.ia.br - Determine suas informações
Showing below up to 50 results in range #16,801 to #16,850.
- Liver neoplastic disease (Q96009)
- Biliary tract neoplasm, not elsewhere classified (Q96008)
- Neoplasm of unknown behaviour of submandibular salivary gland (Q96007)
- Skin of vulva (Q96006)
- Disorder of continuity of bone, neck (Q96005)
- Disorder of continuity of bone, multiple sites (Q96004)
- Other cyst of bone, pelvic region or thigh (Q96003)
- Disorder of continuity of bone, pelvic region or thigh (Q96002)
- Other cyst of bone, ankle or foot (Q96001)
- Disorder of continuity of bone, ribs (Q96000)
- Disorder of continuity of bone, lower leg (Q95999)
- Disorder of continuity of bone, hand (Q95998)
- Disorder of continuity of bone, upper arm (Q95997)
- Disorder of continuity of bone, trunk (Q95996)
- Diastasis of cranial bones (Q95995)
- Other cyst of bone, ribs (Q95994)
- Disorder of continuity of bone, shoulder region (Q95993)
- Other cyst of bone, trunk (Q95992)
- Other cyst of bone, head (Q95991)
- Other cyst of bone, neck (Q95990)
- Disorder of continuity of bone, ankle or foot (Q95989)
- Disorder of continuity of bone, forearm (Q95988)
- Other cyst of bone, vertebral column (Q95987)
- Other cyst of bone, skull (Q95986)
- Other cyst of bone, lower leg (Q95985)
- Parkinson disease LRRK2 gene mutation 12p11.23-q13.11 (Q95984)
- Parkinson disease UCHL-1 gene mutations 4p14 (Q95983)
- Other cyst of bone, hand (Q95982)
- Infantile neuroaxonal dystrophy (Q95981)
- Parkinson disease parkin mutations (Q95980)
- Other cyst of bone, upper arm (Q95979)
- Parkinson disease DJ-1 gene mutations 1p36 (Q95978)
- Neonatal mineral deficiency affecting the skin (Q95977)
- Spasm of fixation (Q95976)
- Simultoagnosia (Q95975)
- Optic ataxia (Q95974)
- Parkinson disease PINK gene mutations (Q95973)
- Blood and urine tests prior to treatment or procedure (Q95972)
- Other cyst of bone, multiple sites (Q95971)
- Parkinson disease ATP13A2 mutations (Q95970)
- Other cyst of bone, forearm (Q95969)
- Parkinson disease synduclein duplications or triplications (Q95968)
- Other cyst of bone, shoulder region (Q95967)
- Parkinson disease synuclein gene mutation 4q21.23 (Q95966)
- Neonatal vitamin deficiency affecting the skin (Q95965)
- Acute dystonic reaction (Q95964)
- Saccadic palsy (Q95963)
- Skin manifestation of other specified neonatal micronutrient excess or toxicity classified elsewhere (Q95962)
- Acquired infectious haemolytic anaemia (Q95961)
- Coeliac artery embolism (Q95960)
