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FA
see
Friedreich ataxia
Fabry disease
Facial Injuries and Disorders
Facio-digito-genital dysplasia
see
Aarskog-Scott syndrome
Facio-genito-popliteal syndrome
see
popliteal pterygium syndrome
faciocutaneoskeletal syndrome
see
Costello syndrome
Faciogenital dysplasia
see
Aarskog-Scott syndrome
faciopalatoosseous syndrome
see
otopalatodigital syndrome type 1
;
otopalatodigital syndrome type 2
Factor II Deficiency
see
prothrombin deficiency
factor V Leiden thrombophilia
Familial Acoustic Neuromas
see
neurofibromatosis type 2
familial adenomatous polyposis
familial Alzheimer disease (FAD)
see
Alzheimer disease
familial apoceruloplasmin deficiency
see
aceruloplasminemia
familial atrial fibrillation
Familial benign giant-cell tumor of the jaw
see
cherubism
Familial Cavernous Hemangioma
see
cerebral cavernous malformation
Familial Cavernous Malformation
see
cerebral cavernous malformation
Familial Cerebral Cavernous Angioma
see
cerebral cavernous malformation
Familial Cerebral Cavernous Malformation
see
cerebral cavernous malformation
familial cold autoinflammatory syndrome
familial dysautonomia
familial encephalopathy with neuroserpin inclusion bodies
Familial Endocrine Adenomatosis
see
multiple endocrine neoplasia
Familial Exostoses
see
hereditary multiple exostoses
Familial fibrous dysplasia of jaw
see
cherubism
familial hemiplegic migraine
Familial Hemochromatosis
see
hemochromatosis
Familial High Density Lipoprotein Deficiency Disease
see
Tangier disease
Familial Hyperkalemic Periodic Paralysis
see
hyperkalemic periodic paralysis
Familial Hypoalphalipoproteinemia
see
Tangier disease
Familial hypobetalipoproteinemia
see
abetalipoproteinemia
Familial Hypokalemic Periodic Paralysis
see
hypokalemic periodic paralysis
Familial incomplete male pseudohermaphroditism, type 2
see
5-alpha reductase deficiency
familial isolated vitamin E deficiency
see
ataxia with vitamin E deficiency
familial lipoprotein lipase deficiency
familial Mediterranean fever
Familial multilocular cystic disease of the jaws
see
cherubism
familial nodular heterotopia
see
periventricular heterotopia
Familial nonpolyposis colon cancer
see
Lynch syndrome
familial paroxysmal nonkinesigenic dyskinesia
familial pressure sensitive neuropathy
see
hereditary neuropathy with liability to pressure palsies
familial primary pulmonary hypertension
see
pulmonary arterial hypertension
Familial Thrombotic Thrombocytopenia Purpura
see
thrombotic thrombocytopenic purpura
familial tremor
see
essential tremor
familial Turner syndrome
see
Noonan syndrome
Familial vascular leukoencephalopathy
see
cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy
familial veno-occlusive disease with immunodeficiency
see
hepatic veno-occlusive disease with immunodeficiency
Familial Xanthomatosis
see
Wolman disease
FAP
see
familial adenomatous polyposis
Farber lipogranulomatosis
FCAS
see
familial cold autoinflammatory syndrome
FCMD
see
Fukuyama congenital muscular dystrophy
FCS syndrome
see
Costello syndrome
FCU
see
familial cold autoinflammatory syndrome
FD
see
familial dysautonomia
female pattern baldness
see
androgenetic alopecia
Female Pseudo-Turner Syndrome
see
Noonan syndrome
FENIB
see
familial encephalopathy with neuroserpin inclusion bodies
ferritin-related neurodegeneration
see
neuroferritinopathy
Fetal face syndrome
see
Robinow syndrome
Fetal iritis syndrome
see
Norrie disease
Fever
FG syndrome
FGFR3-associated coronal synostosis
see
Muenke syndrome
fibrinoid degeneration of astrocytes
see
Alexander disease
Fibrocystic Disease of Pancreas
see
cystic fibrosis
fibrodysplasia ossificans progressiva
Fibrofolliculomas with trichodiscomas and acrochordons
see
Birt-Hogg-Dubé syndrome
Fibrous Dysplasia, Polyostotic
see
McCune-Albright syndrome
Fibrous dysplasia with pigmentary skin changes and precocious puberty
see
McCune-Albright syndrome
Fish malodor syndrome
see
trimethylaminuria
Fish odor syndrome
see
trimethylaminuria
FIVE
see
ataxia with vitamin E deficiency
FMF
see
familial Mediterranean fever
Folling Disease
see
phenylketonuria
Fong disease
see
nail-patella syndrome
Foot Injuries and Disorders
see
hand-foot-genital syndrome
foramina parietalia permagna
see
enlarged parietal foramina
FPO
see
otopalatodigital syndrome type 1
;
otopalatodigital syndrome type 2
FPP
see
enlarged parietal foramina
FPPH
see
pulmonary arterial hypertension
fra(X) syndrome
see
fragile X syndrome
fragile X syndrome
Fragilitas ossium
see
osteogenesis imperfecta
Franceschetti-Zwahlen-Klein syndrome
see
Treacher Collins syndrome
FRAXA Syndrome
see
fragile X syndrome
FRDA
see
Friedreich ataxia
free sialic acid storage disease
see
sialic acid storage disease
French type sialuria
see
sialuria
Friedreich ataxia
Friedreich ataxia phenotype with selective vitamin E deficiency
see
ataxia with vitamin E deficiency
Friedreich-like ataxia
see
ataxia with vitamin E deficiency
Friedreich's Ataxia
see
ataxia-telangiectasia
;
ataxia with oculomotor apraxia
;
autosomal recessive spastic ataxia of Charlevoix-Saguenay
;
episodic ataxia
;
Friedreich ataxia
frontometaphyseal dysplasia
Fucosidase deficiency
see
fucosidosis
fucosidosis
Fukuyama congenital muscular dystrophy
fumarase deficiency
fumarate hydratase deficiency
see
fumarase deficiency
fumaric aciduria
see
fumarase deficiency
FXS
see
fragile X syndrome
Published: January 23, 2009