Atlas Médico

Accessible medical knowledge

All Diseases

Familial cold autoinflammatory syndrome 2

Familial cold autoinflammatory syndrome 3

Familial cold autoinflammatory syndrome 4

Familial colorectal cancer

Familial colorectal cancer type X

Familial congenital mirror movements

Familial congenital palsy of trochlear nerve

Familial cutaneous collagenoma

Familial cystic renal disease

Familial dermatographia

Familial developmental dysphasia

Familial digital arthropathy-brachydactyly

Familial dilated cardiomyopathy

Familial Dupuytren contracture

Familial dysfibrinogenemia

Familial encephalopathy with neuroserpin inclusion bodies

Familial episodic pain syndrome with predominantly lower limb involvement

Familial focal epilepsy with variable foci

Familial generalized lentiginosis

Familial glucocorticoid deficiency

Familial hemiplegic migraine

Familial hemolytic anemia

Familial hemophagocytic lymphohistiocytosis 2

Familial hemophagocytic lymphohistiocytosis 3

Familial hemophagocytic lymphohistiocytosis 4

Familial hemophagocytic lymphohistiocytosis 5

Familial hemophagocytic lymphohistiocytosis type 1

Familial hyperaldosteronism

Familial hyperaldosteronism type II

Familial hyperaldosteronism type III

Familial hypercholesterolemia

Familial hyperinsulinism

Familial hyperlipidemia

Familial hyperprolactinemia

Familial hyperthyroidism due to mutations in TSH receptor

Familial hypertrophic cardiomyopathy

Familial hypertryptophanemia

Familial hypoaldosteronism

Familial hypobetalipoproteinemia 1

Familial hypobetalipoproteinemia 2

Familial hypocalciuric hypercalcemia

Familial hypocalciuric hypercalcemia 1

Familial hypocalciuric hypercalcemia 2

Familial hypocalciuric hypercalcemia 3

Familial hypofibrinogenemia

Familial hypoparathyroidism

Familial idiopathic dilatation of the right atrium

Familial idiopathic inflammatory myopathy

Familial idiopathic steroid-resistant nephrotic syndrome

Familial idiopathic torsion dystonia

Familial infantile bilateral striatal necrosis

Familial infantile myoclonic epilepsy

Familial intrahepatic cholestasis

Familial isolated arrhythmogenic right ventricular dysplasia

Familial isolated clinodactyly of fingers

Familial isolated congenital asplenia

Familial isolated deficiency of vitamin E

Familial isolated dilated cardiomyopathy

Familial isolated hyperparathyroidism

Familial isolated hypoparathyroidism due to agenesis of parathyroid gland

Familial isolated trichomegaly

Familial juvenile hypertrophy of the breast

Familial juvenile hyperuricemic nephropathy type 1

Familial juvenile hyperuricemic nephropathy type 2

Familial keratoacanthoma

Familial lipoprotein lipase deficiency

Familial long QT syndrome

Familial male-limited precocious puberty

Familial median cleft of the upper and lower lips

Familial Mediterranean fever

Familial medullary thyroid carcinoma

Familial melanoma

Familial meningioma

Familial mesial temporal lobe epilepsy

Familial mitral valve prolapse

Familial monosomy 7 syndrome

Familial multiple discoid fibromas

Familial multiple fibrofolliculoma

Familial multiple lipomatosis

Familial multiple meningioma

Familial multiple nevi flammei

Familial nasal acilia

Familial nephrotic syndrome

Familial nonmedullary thyroid carcinoma

Familial omphalocele syndrome with facial dysmorphism

Familial or sporadic hemiplegic migraine

Familial ossifying fibroma

Familial osteodysplasia, Anderson type

Familial osteosclerosis

Familial ovarian cancer

Familial ovarian carcinoma

Familial pancreatic carcinoma

Familial papillary or follicular thyroid carcinoma

Familial papillary thyroid carcinoma with renal papillary neoplasia

Familial parathyroid adenoma

Familial partial epilepsy

Familial partial lipodystrophy

Familial partial lipodystrophy, Dunnigan type

Familial partial lipodystrophy, Kobberling type

Familial periodic paralysis