Atlas Médico

Accessible medical knowledge

All Diseases

Familial pityriasis rubra pilaris

Familial polycythemia

Familial porencephaly

Familial porphyria cutanea tarda

Familial primary hyperparathyroidism

Familial primary hypomagnesemia

Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis

Familial primary hypomagnesemia with normocalciuria and normocalcemia

Familial primary hypomagnesemia with normocalcuria

Familial primary pulmonary hypoplasia

Familial progressive hyper- and hypopigmentation

Familial progressive hyperpigmentation

Familial prostate carcinoma

Familial pseudohyperkalemia

Familial pterygium of the conjunctiva

Familial reactive perforating collagenosis

Familial renal glucosuria

Familial restrictive cardiomyopathy

Familial rhabdoid tumor

Familial scaphocephaly syndrome, McGillivray type

Familial schizencephaly

Familial sick sinus syndrome

Familial sleep-related hypermotor epilepsy

Familial spontaneous pneumothorax

Familial supernumerary nipples

Familial syringomyelia

Familial temporal lobe epilepsy 2

Familial temporal lobe epilepsy 4

Familial temporal lobe epilepsy 5

Familial temporal lobe epilepsy 6

Familial temporal lobe epilepsy 7

Familial temporal lobe epilepsy 8

Familial thoracic aortic aneurysm and aortic dissection

Familial thrombocytosis

Familial thyroglossal duct cyst

Familial thyroid dyshormonogenesis

Familial tumoral calcinosis

Familial vesicoureteral reflux

Familial visceral myopathy

Famililal cerebral cavernous malformations

FANCM Fanconi-like genomic instability disorder

Fanconi anemia

Fanconi anemia complementation group A

Fanconi anemia complementation group B

Fanconi anemia complementation group C

Fanconi anemia complementation group D1

Fanconi anemia complementation group D2

Fanconi anemia complementation group E

Fanconi anemia complementation group F

Fanconi anemia complementation group G

Fanconi anemia complementation group I

Fanconi anemia complementation group J

Fanconi anemia complementation group L

Fanconi anemia complementation group N

Fanconi anemia complementation group O

Fanconi anemia complementation group P

Fanconi anemia complementation group Q

Fanconi anemia complementation group R

Fanconi anemia complementation group T

Fanconi anemia complementation group U

Fanconi anemia complementation group V

Fanconi renotubular syndrome

Fanconi renotubular syndrome 2

Fanconi renotubular syndrome 3

Fanconi renotubular syndrome 4 with maturity-onset diabetes of the young

Fanconi-like syndrome

Far-East scarlet-like fever

Farber lipogranulomatosis

Farmer's lung disease

FAS-related autoimmune lymphoproliferative immune disorder

Fasciitis

Fascioliasis

Fascioloidiasis

Fasciolopsiasis

FASLG-related immunodeficiency

Fat necrosis of breast

FAT4-related neurodevelopmental disorder

Fatal familial insomnia

Fatal infantile encephalocardiomyopathy

Fatal mitochondrial disease due to combined oxidative phosphorylation defect type 3

Fatal multiple mitochondrial dysfunctions syndrome

Fatty acid hydroxylase-associated neurodegeneration

Fatty acyl-CoA reductase 1 deficiency

Fatty acyl-CoA reductase 1 upregulation

Fatty acyl-CoA reductase defects

Fatty liver disease

Faucial diphtheria

Favism

FDXR-related optic atrophy mitochondrial dysfunction syndrome

Febrile infection-related epilepsy syndrome

Febrile seizures, familial, 4

Febrile seizures, familial, 8

Febrile ulceronecrotic Mucha-Habermann disease

Feingold syndrome

Feingold syndrome type 1

Feingold syndrome type 2

Felty syndrome

Female breast axillary tail cancer

Female breast carcinoma

Female genital tuberculosis