Rare Disease Library

Familial hyperaldosteronism

FH

Facial dysmorphism-hypertrichosis-epilepsy-intellectual disability/developmental delay-gingival overgrowth syndrome

FHEIG syndrome

Faisalabad histiocytosis

FHC

Familial hyperaldosteronism type I

Dexamethasone-sensitive hypertension · FH-I

Familial hyperaldosteronism type II

FH-II · FH2

Familial hyperaldosteronism type III

FH-III · FH3

Familial hyperaldosteronism type IV

FH4

Familial hyperinsulinism

FHI · Familial hyperinsulinemic hypoglycemia

Familial hypocalciuric hypercalcemia

FBH · FBHH

Familial hypocalciuric hypercalcemia type 1

FHH type 1

Familial hypocalciuric hypercalcemia type 2

FHH type 2

Familial hypocalciuric hypercalcemia type 3

FHH type 3

Femoral-facial syndrome

FFS · FHUFS

Fibrolamellar hepatocellular carcinoma

FHCC · Fibrolamellar hepatocarcinoma

Foveal hypoplasia-optic nerve decussation defect-anterior segment dysgenesis syndrome

FHONDA syndrome

Fuchs heterochromic iridocyclitis

FHI

Primary hypomagnesemia with hypercalciuria and nephrocalcinosis

FHHNC · Michellis-Castrillo syndrome

Primary hypomagnesemia with hypercalciuria and nephrocalcinosis with severe ocular involvement

FHHNC with severe ocular involvement · Hypercalciuria-bilateral macular coloboma syndrome

Primary hypomagnesemia with hypercalciuria and nephrocalcinosis without severe ocular involvement

FHHNC without severe ocular involvement · HOMG3