Symptoms

Type 1 and type 2 muscle fiber minicore regions

Type 1 collagen overmodification

Type 1 congenital pulmonary airway malformation

Type 1 diabetes

Type 1 fibers relatively smaller than type 2 fibers

Type 1 muscle fiber atrophy

Type 1 muscle fiber predominance

Type 1 schizencephaly

Type 2 Diabetes

Type 2 congenital pulmonary airway malformation

Type 2 muscle fiber atrophy

Type 2 muscle fiber predominance

Type 2 schizencephaly

Type 3 congenital pulmonary airway malformation

Type 3 schizencephaly

Type A brachydactyly

Type A1 brachydactyly

Type A2 brachydactyly

Type A4 brachydactyly

Type A5 brachydactyly

Type B brachydactyly

Type C brachydactyly

Type D brachydactyly

Type E brachydactyly

Type I atherosclerotic lesion

Type I cryptotia

Type I diabetes mellitus

Type I radial ray deficiency

Type I transferrin isoform profile

Type I truncus arteriosus

Type II atherosclerotic lesion

Type II cryptotia

Type II diabetes mellitus

Type II lissencephaly

Type II pneumocyte hyperplasia

Type II pneumocyte hypertrophy

Type II radial ray deficiency

Type II transferrin isoform profile

Type II truncus arteriosus

Type III atherosclerotic lesion

Type III radial ray deficiency

Type III truncus arteriosus

Type IV atherosclerotic lesion

Type IV radial ray deficiency

Type IV truncus arteriosus

Type V atherosclerotic lesion

Type VI atherosclerotic lesion

Typical absence seizure

Typical absence status epilepticus

Typical atrial flutter

Typical perifissural nodule

Typically de novo

Typically symptoms start around age...

Typically thumb index and middle...

Typified by age-related disease onset

Typified by complete penetrance

Typified by high penetrance

Typified by highly variable age of onset

Typified by incomplete penetrance

Typified by low penetrance

Typified by moderate penetrance

Typified by somatic mosaicism

Tyrosinuria

Tzanck smear with multinucleated giant cells