familial metaphyseal dysostosis
familial metaphyseal dysostosis
(1) Metaphyseal chondrodysplasia (Jansen type), OMIM:156400.(2) Metaphyseal chondrodysplasis (Schmid type), OMIM:156500.
(2) Metaphyseal chondrodysplasis (Schmid type), OMIM:156500.
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- familial hypercholesterolemia
- familial hypercholesterolemic xanthomatosis
- familial hyperchylomicronemia
- familial hyperlipoproteinemia
- familial hyperlipoproteinemia type I
- familial hyperlipoproteinemia type II
- familial hyperlipoproteinemia type III
- familial hyperlipoproteinemia type IV
- familial hyperlipoproteinemia type V
- familial hyperproinsulinaemia
- familial hypertriglyceridemia
- familial hypertrophic cardiomyopathy
- familial hypobetalipoproteinemia
- familial hypogonadotropic hypogonadism
- familial hypoparathyroidism
- familial hypoproteinaemia-lymphangiectatic enteropathy
- familial intestinal polyposis
- familial intraosseous fibrous swelling of the jaws
- familial juvenile nephronophthisis
- familial juvenile nephrophthisis
- familial lipoprotein lipase inhibitor
- familial malignancy
- familial Mediterranean fever
- familial Mediterranean fever, autosomal dominant
- familial medullary thyroid cancer
- familial metaphyseal dysostosis
- familial microcytic anemia
- familial nephrosis
- familial nonhemolytic jaundice
- familial osteochondrodystrophy
- familial paroxysmal polyserositis
- familial paroxysmal rhabdomyolysis
- familial partial lipodystrophy
- familial partial lipodystrophy type 3
- familial periodic fever
- familial periodic paralysis
- familial polyendocrine adenomatosis
- familial polyposis
- familial porphyria cutanea tarda
- familial progressive hyperpigmentation
- familial pseudoinflammatory macular degeneration
- familial pseudoinflammatory maculopathy
- familial pyridoxine-responsive anemia
- familial recurrent polyserositis
- familial screening
- familial short stature
- familial spinal muscular atrophy
- familial spinal neurofibromatosis
- familial tremor
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- Family and Medical Leave Act
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- familial juvenile nephrophthisis
- Familial Juvenile Polyposis
- familial lipoprotein deficiency
- familial lipoprotein deficiency
- familial lipoprotein deficiency
- familial lipoprotein deficiency
- familial lipoprotein deficiency
- familial lipoprotein deficiency
- familial lipoprotein lipase inhibitor
- Familial long QT syndrome
- Familial Low Tone Deafness
- Familial male precocious puberty
- familial malignancy
- Familial MCT
- Familial Mediteranian Fever
- Familial Mediteranian Fever
- familial Mediterranean fever
- familial Mediterranean fever
- familial Mediterranean fever
- familial Mediterranean fever
- familial Mediterranean fever
- Familial Mediterranean Fever Gene
- familial Mediterranean fever, autosomal dominant
- Familial Medullary Thyroid Cancer
- Familial Medullary Thyroid Cancer
- Familial Medullary Thyroid Cancer
- Familial Medullary Thyroid Cancer
- Familial Medullary Thyroid Cancer
- Familial Mental Retardation Protein
- Familial mesial temporal lobe epilepsy
- familial metaphyseal dysostosis
- familial microcytic anemia
- Familial Multilocular Cystic Disease of The Jaw
- Familial Multilocular Cystic Disease of The Jaw
- Familial multilocular cystic disease of the jaws
- Familial multilocular cystic disease of the jaws
- Familial Multilocular Cystic Jaw Disease
- Familial Multilocular Cystic Jaw Disease
- Familial Multiple Coagulation Factor Deficiency
- familial multiple endocrine adenomatosis
- Familial Multiple Endocrine Neoplasia
- Familial Multiple Endocrine Neoplasia Type 1
- familial myoclonic epilepsy
- familial myoclonic epilepsy
- familial myoclonic epilepsy
- familial myoclonic epilepsy
- familial myositis
- familial myositis
- familial myositis
- Familial Neonatal Convulsion
- Familial Neonatal Seizures
- familial nephropathy
- familial nephropathy
- familial nephropathy
- familial nephropathy with gout
- familial nephrosis
- Familial Neurohypophysial Diabetes Insipidus
- familial neuroviscerolipidosis
- familial neuroviscerolipidosis
- familial non-haemolytic bilirubinaemia
- familial non-haemolytic cholaemia
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