Enfermedades y tipo de herencia

Question 1

POLIQUISTOSIS RENAL DEL ADULTO

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AD

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XD

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Question 2

COREA DE HUNTINGTON

Accepted Answer

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Question 3

MIOCARDIOPATÍA HIPERTRÓFICA HEREDITARIA

Accepted Answer

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Question 4

DISTROFIA MIOTÓNICA DE STEINERT

Accepted Answer

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Question 5

OTOESCLEROSIS

Accepted Answer

AD

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Question 6

ENFERMEDAD DE VON WILLEBRAND MÁS FRECUENTE

Accepted Answer

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Question 7

DIABETES TIPO MODY

Accepted Answer

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Question 8

ATAXIA ESPINOCEREBELAR TIPO 3 (SC3)

Accepted Answer

AD

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Question 9

CHARCOT-MARIE-TOOTH TIPO 2A

Accepted Answer

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Question 10

RENDU OSLER

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Question 11

MEN 1 Y 2

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Question 12

NEUROFIBROMATOSIS TIPO 1 Y TIPO 2

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Question 13

ESCLEROSIS TUBEROSA  (BOURNEVILLE)

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Question 14

VON HIPPEL LINDAU

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Question 15

HIPERCOLESTEROLEMIA FAMILIAR / HIPERTRIGLICERIDEMIA FAMILIAR

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Question 16

LYNCH (CÁNCER DE COLON HEREDITARIO SIN POLIPOSIS)

Accepted Answer

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Question 17

CÁNCER DE MAMA Y OVARIO HEREDITARIO (BRCA+)

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Question 18

POLIPOSIS COLÓNICA FAMILIAR

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Question 19

ESFEROCITOSIS HEREDITARIA

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Question 20

ENFERMEDAD DE MARFAN

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Question 21

OSTEOGÉNESIS IMPERFECTA

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Question 22

ICTIOSIS VULGAR

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Question 23

DÉFICIT DE PROTEÍNA C / DÉFICIT DE PROTEÍNA S /DÉFICIT DE ANTITROMBINA III

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Question 24

FACTOR V LEIDEN (RESISTENCIA A LA PROTEÍNA C ACTIVADA)

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Question 25

FIBROSIS QUÍSTICA

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Question 26

HEMOCROMATOSIS

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Question 27

ATAXIA DE FRIEDREICH

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Question 28

ATAXIA TELANGIECTASIA

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Question 29

XERODERMA PIGMENTOSO

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Question 30

ANEMIA DE FANCONI

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Question 31

SÍNDROME DE BARTTER

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Question 32

ENFERMEDAD DE WILSON

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Question 33

DÉFICIT DE ALFA1- ANTITRIPSINA

Accepted Answer

Codominante

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Question 34

DÉFICIT DE 21-ALFA-HIDROXILASA

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Question 35

DEFECTOS METABÓLICO-ENZIMÁTICOS (EXCEPTO FABRY Y HUNTER)

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Question 36

FABRY / HUNTER

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Question 37

RAQUITISMO VITAMINO-RESISTENTE (HIPOFOSFATEMIA)

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Question 38

INCONTINENCIA PIGMENTI

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Question 39

SÍNDROME DE ALPORT

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Question 40

HIPERAMONIEMIA POR DÉFICIT DE ORNITINA TRANSCARBAMILASA

Accepted Answer

XD

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Question 41

CHARCOT-MARIE TOOTH TIPO 1X

Accepted Answer

XD/XR

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Question 42

MIOPATÍA DE DUCHENE Y BECKER

Accepted Answer

XR

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Question 43

HEMOFILIA A Y B

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Question 44

DEFICIENCIA DE GLUCOSA 6 FOSFATO DESHIDROGENASA

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Question 45

ENFERMEDAD GRANULOMATOSA CRÓNICA

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Question 46

WISKOTT-ALDRICH

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Question 47

HIPOGAMMAGLOBULINEMIA DE BRUTON

Accepted Answer

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Question 48

X FRÁGIL

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Question 49

SÍNDROME DE LESCH-NYHAN

Accepted Answer

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Question 50

DALTONISMO

Accepted Answer

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Question 51

SÍNDROME DE MORRIS

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Question 52

DIABETES INSÍPIDA NEFROGÉNICA FAMILIAR

Accepted Answer

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Question 53

NEUROPATÍA ÓPTICA DE LEBER

Accepted Answer

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Question 54

MERRF (EPILEPSIA MIOCLÓNICA DE FIBRAS ROJAS ROTAS)

Accepted Answer

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Question 55

MELAS

Accepted Answer

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Question 56

SÍNDROME DE NEUROPATÍA Y RETINITIS PIGMENTARIA

Accepted Answer

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Question 57

SÍNDROME DE PEARSON

Accepted Answer

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Question 58

SÍNDROME DE KEARNS-SAYRE

Accepted Answer

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Question 59

FIEBRE MEDITERRÁNEA FAMILIAR

Accepted Answer

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Answer

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	Creado por Alberto Hernandez hace casi 6 años

Siguiente

Enfermedades y tipo de herencia

Descripción

Resumen del Recurso

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