Search Diseases
???pagination.result.count???
???pagination.result.page??? ???pagination.result.prev??? 1 2 3 4 5 6 7 8 9 10 11 ???pagination.result.next???
Disease | Synonyms | Description | Articles | Phenotypes |
---|---|---|---|---|
Feingold syndrome |
FGLDS; digital anomalies with short palpebral fiss..
[+]
|
A syndrome characterized by variable combinations ..[+]
|
||
fibrochondrogenesis |
|
n_a
|
||
fetal valproate syndrome |
fetal valproic acid syndrome
|
A syndrome characterized by distinctive facial app..[+]
|
||
familial erythrocytosis 2 |
familial erythrocytosis 2; autosomal recessive ben..
[+]
|
A primary polycythemia that has_material_basis_in ..[+]
|
||
fruit allergy |
|
A food allergy triggered by a plant fruit product.
|
||
fish allergy |
|
A food allergy triggered by fish.
|
||
fetal nicotine spectrum disorder |
|
A specific developmental disorder that is characte..[+]
|
||
fetal encasement syndrome |
fetal encasement syndrome; cocoon syndrome
|
A syndrome that has_material_basis_in homozygous m..[+]
|
||
familial erythrocytosis 1 |
autosomal dominant benign erythrocytosis; primary ..
[+]
|
A primary polycythemia that has_material_basis_in ..[+]
|
||
familial hypocalciuric hypercalcemia |
A hypercalcemia characterized byautosomal dominant..[+]
|
|||
familial hypocalciuric hypercalcemia 1 |
A familial hypocalciuric hypercalcemia that has_ma..[+]
|
|||
familial hypocalciuric hypercalcemia 2 |
A familial hypocalciuric hypercalcemia that has_ma..[+]
|
|||
familial hypocalciuric hypercalcemia 3 |
A familial hypocalciuric hypercalcemia that has_ma..[+]
|
|||
familial temporal lobe epilepsy 1 |
ETL1; partial epilepsy with auditory features
|
A temporal lobe epilepsy characterized by autosoma..[+]
|
||
familial temporal lobe epilepsy 6 |
ETL6
|
A temporal lobe epilepsy that has_material_basis_i..[+]
|
||
familial temporal lobe epilepsy 3 |
FMTLE; familial mesial temporal lobe epilepsy
|
A temporal lobe epilepsy characterized by simple o..[+]
|
||
familial temporal lobe epilepsy 7 |
ETL7
|
A temporal lobe epilepsy characterized by autosoma..[+]
|
||
familial temporal lobe epilepsy 5 |
ETL5
|
A temporal lobe epilepsy that has_material_basis_i..[+]
|
||
familial temporal lobe epilepsy 4 |
EPOLM; ETL4; occipitotemporal lobe epilepsy and mi..
[+]
|
A temporal lobe epilepsy characterized by autosoma..[+]
|
||
familial temporal lobe epilepsy 8 |
ETL8
|
A temporal lobe epilepsy characterized by autosoma..[+]
|
||
familial temporal lobe epilepsy 2 |
ETL2
|
A temporal lobe epilepsy characterized by autosoma..[+]
|
||
familial chronic myelocytic leukemia-like syndrome |
familial CML-like syndrome
|
A chronic myeloid leukemia characterized by chroni..[+]
|
||
familial partial lipodystrophy type 5 |
A familial partial lipodystrophy characterized by ..[+]
|
|||
familial hyperinsulinemic hypoglycemia 7 |
EIHI; exercise-induced hyperinsulinemic hypoglycem..
[+]
|
A hyperinsulinemic hypoglycemia characterized by a..[+]
|
||
fibrous dysplasia |
|
A bone remodeling disease that results_in the dest..[+]
|
||
fibrogenesis imperfecta ossium |
Baker's disease
|
A syndrome that involves abnormality of collagen s..[+]
|
||
familial erythrocytosis 5 |
ECYT5
|
A primary polycythemia characterized by autosomal ..[+]
|
||
familial erythrocytosis 3 |
ECYT3
|
A primary polycythemia that has_material_basis_in ..[+]
|
||
familial adenomatous polyposis 3 |
|
A familial adenomatous polyposis that has_material..[+]
|
||
familial glucocorticoid deficiency |
|
An adrenal cortex disease that is characterized by..[+]
|
||
fibrochondrogenesis 1 |
|
A fibrochondrogenesis that is characterized by a f..[+]
|
||
Fanconi renotubular syndrome 1 |
|
A Fanconi syndrome that has_material_basis_in hete..[+]
|
||
Fanconi renotubular syndrome 5 |
Acadian-variant Fanconi syndrome
|
A Fanconi syndrome that is characterized by proxim..[+]
|
||
frontonasal dysplasia |
|
A syndrome that is a cleft in thes nose, a broad n..[+]
|
||
familial hyperinsulinemic hypoglycemia 8 |
|
A hyperinsulinemic hypoglycemia characterized by p..[+]
|
||
Fraser syndrome |
cryptophthalmos with other malformations
|
An autosomal recessive disease characterized by cr..[+]
|
||
familial isolated deficiency of vitamin E |
familial isolated vitamin E deficiency; ataxia wit..
[+]
|
A vitamin metabolic disorder characterized by prog..[+]
|
||
familial cold autoinflammatory syndrome |
|
A primary immunodeficiency disease characterized b..[+]
|
||
familial cold autoinflammatory syndrome 1 |
|
A familial cold autoinflammatory syndrome characte..[+]
|
||
familial cold autoinflammatory syndrome 2 |
NLRP12-associated hereditary periodic fever syndro..
[+]
|
A familial cold autoinflammatory syndrome characte..[+]
|
||
familial cold autoinflammatory syndrome 3 |
|
A familial cold autoinflammatory syndrome characte..[+]
|
||
familial cold autoinflammatory syndrome 4 |
|
A familial cold autoinflammatory syndrome characte..[+]
|
||
Fanconi-like syndrome |
|
A syndrome characterized by pancytopenia, immune d..[+]
|
||
Fuhrmann syndrome |
|
A bone development disease characterized by autoso..[+]
|
||
frontotemporal dementia and/or amyotrophic lateral sclerosis-3 |
An amyotrophic lateral sclerosis that has_material..[+]
|
|||
FTDALS4 |
frontotemporal dementia and/or amyotrophic lateral..
[+]
|
An amyotrophic lateral sclerosis that has material..[+]
|
||
familial hemophagocytic lymphohistiocytosis 1 |
FHL1; HLH1; HPLH1
|
A hemophagocytic lymphohistiocytosis that has_mate..[+]
|
||
familial hemophagocytic lymphohistiocytosis 2 |
FHL2; HLH2; HPLH2
|
A hemophagocytic lymphohistiocytosis that has_mate..[+]
|
||
familial hemophagocytic lymphohistiocytosis 3 |
FHL3; HLH3; HPLH3
|
A hemophagocytic lymphohistiocytosis that has_mate..[+]
|
||
familial hemophagocytic lymphohistiocytosis 4 |
FHL4; HLH4; HPLH4
|
A hemophagocytic lymphohistiocytosis that has_mate..[+]
|
???pagination.result.page??? ???pagination.result.prev??? 1 2 3 4 5 6 7 8 9 10 11 ???pagination.result.next???