C2750440 |
FATTY LIVER DISEASE, NONALCOHOLIC, SUSCEPTIBILITY TO, 1
|
disease |
|
Finding
|
genetic disease; disease of metabolism
|
|
63 |
C2750441 |
LIVER DISEASE, ALCOHOLIC, SUSCEPTIBILITY TO, 1
|
phenotype |
|
Finding
|
genetic disease; disease of metabolism
|
|
63 |
C3150651 |
FATTY LIVER DISEASE, NONALCOHOLIC, SUSCEPTIBILITY TO, 2
|
phenotype |
|
Finding
|
genetic disease; disease of metabolism
|
|
63 |
C0018129 |
Graft Rejection
|
phenotype |
|
Organ or Tissue Function
|
|
|
47 |
C1415817 |
HETEROTAXY, VISCERAL, 2, AUTOSOMAL
|
disease |
|
Disease or Syndrome
|
physical disorder
|
|
29 |
C3151057 |
HETEROTAXY, VISCERAL, 4, AUTOSOMAL
|
disease |
|
Disease or Syndrome
|
physical disorder
|
|
29 |
C3151867 |
CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED
|
disease |
|
Disease or Syndrome
|
physical disorder
|
|
29 |
C3553676 |
HETEROTAXY, VISCERAL, 6, AUTOSOMAL
|
disease |
|
Disease or Syndrome
|
physical disorder
|
|
29 |
C1408174 |
Hypertrophic neuropathy of infancy
|
disease |
|
Disease or Syndrome
|
genetic disease; disease of anatomical entity
|
|
21 |
C1408182 |
Hereditary motor and sensory neuropathy, types I-IV
|
disease |
|
Disease or Syndrome
|
genetic disease; disease of anatomical entity
|
|
21 |
C2875300 |
Peroneal muscular atrophy (axonal type) (hypertrophic type)
|
disease |
|
Disease or Syndrome
|
genetic disease; disease of anatomical entity
|
|
21 |
C1397307 |
Cardiac fibrosis
|
disease |
|
Disease or Syndrome
|
|
|
17 |
C0869083 |
Other specified congenital malformation syndromes, not elsewhere classified in ICD10CM
|
disease |
|
Disease or Syndrome
|
genetic disease; disease of anatomical entity; syndrome; disease of mental health; physical disorder
|
|
14 |
C1333419 |
Liver and Intrahepatic Bile Duct Epithelial Neoplasm
|
disease |
|
Neoplastic Process
|
disease of anatomical entity; disease of cellular proliferation
|
|
12 |
C2875316 |
Myotubular (centronuclear) myopathy
|
disease |
|
Congenital Abnormality
|
genetic disease; disease of anatomical entity
|
|
9 |
C0342381 |
Idiopathic growth hormone deficiency
|
disease |
|
Disease or Syndrome
|
genetic disease; disease of anatomical entity
|
|
8 |
C2874188 |
Isolated deficiency of pituitary hormone
|
disease |
|
Disease or Syndrome
|
genetic disease; disease of anatomical entity
|
|
8 |
C2874189 |
Necrosis of pituitary gland (postpartum)
|
phenotype |
|
Pathologic Function
|
genetic disease; disease of anatomical entity
|
|
8 |
C2874190 |
Pituitary short stature
|
disease |
|
Disease or Syndrome
|
genetic disease; disease of anatomical entity
|
|
8 |
C0334096 |
Intimal proliferation
|
phenotype |
|
Pathologic Function
|
|
|
7 |
C1096249 |
Calcification of the aorta
|
phenotype |
|
Pathologic Function
|
|
Abnormality of the skeletal system; Abnormality of the cardiovascular system
|
6 |
C1868773 |
Diabetic encephalopathy
|
disease |
|
Disease or Syndrome
|
|
|
6 |
C2751052 |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITHOUT MENTAL RETARDATION), TYPE B, 4
|
disease |
|
Disease or Syndrome
|
genetic disease; disease of anatomical entity
|
|
6 |
C2945695 |
Limb ischemia
|
disease |
|
Disease or Syndrome
|
|
|
6 |
C3150412 |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 3
|
disease |
|
Disease or Syndrome
|
genetic disease; disease of anatomical entity
|
|
6 |