| blood sexual | familial tremor | blood character disease |
| familial adiposity | Familial Olfactory nerve | familial ova-rian |
| familial cretinism | familial polyposis | familial myocardosis |
| Familial Macrognathia disease | familial Mediterranean fever | familial polyp of colon |
| familial allergy | innocence Familial haematuria | familial intestinal polyposis |
| Familial dwarfishness build | Familial innocence haematuria | familial short in stature |
| Familial circularity erythema | familial Cold hives | familial leukodystrophy |
| familial ligament flab | familial periodic paralysis | familial adenomatous polyposis |
| familial spastic paraplegia | familial amaurotic idiocy | chronicity Familial pemphigus |
| familial Base burl calcification | innocence Familial ballismus | familial polyposis coli |
| Familial contradict syndrome | familial visual nerve atresia | familial Tangshi syndrome |
| familial Hyperlipidaemia model | Familial model hyperlipidaemia | Familial across Lipoprotein illness |
| Familial fat White deficiency | Familial Daixiao deaf dumbness | familial Cartilage calcium aplomb |
| Familial chemotaxis defect | familial Myocardial hypertrophy disease | Familial lipoprotein defect |
| familial Lipoprotein Hyperlipidemia | Familial Flow nature nephritis | Familial The _drop_ serene=(the serene _drop_) character amentia |
| Familial innocence pemphigus | Familial Bark Collagen neoplasm | familial down syndrome |
| familial dysautonomia | familial progressive spinal muscular atrophy | Kuf disease |
| Bielschowsky disease | alpha-Lipoprotein Deficiency Disease, Familial | dysautonomia |
| dysautonomia | familial Male gonad action lowness disease | Familial innocence Granulocytopenia disease |
| Familial Non- hemolytic jaundice | Familial Adenoma character polyposis | innocence Familial Intrahepatic cholestasis disease |
| Familial Transmissibility male neoteny | innocence Familial new Sheng'er convulsions | Familial Amylum appearance more Bundle become |
| Familial Duofaxing polyp of colon | Familial Freedom Bundle Ailment disease | Lethality familial insomnia |
| Familial second amidogen glycinuria | familial hypercholesterolemia | familial Cerebellar cortex atresia syndrome |
| familial Gynaecomastia syndrome | culture Familial mental retardation | familial polyposis coli remedy |
| Familial compounding hyperlipidaemia | Familial Gaoqian Lipoprotein Hyperlipidemia | Familial Lipoprotein Guoshaoxuezheng |
| Familial Zaizhi White deficiency | Familial fat Kwashiorkor | Familial Dizhi egg leukaemia |
| familial hyperlipaemia | Familial blood Lipoprotein Abnormal disease | Familial model hyperlipaemia |
| Familial across hyperlipaemia | Familial abnormal Lipoprotein Hyperlipidemia | familial low Lipoprotein Hyperlipidemia |
| familial Apolipoprotein Defect disease | Duofaxing Familial polyp of colon | Familial Zhangzhi hyperkeratosis |
| Familial Breeding badness character anaemia | Familial Conduct System barrier | Idiopathic familial hyperlipidaemia |
| Familial idiopathic paramyoclonus | Familial whole Marrow aplasia | Familial Mixture nature hyperlipidaemia |
| Familial Innocence chronicity pemphigus | familial pancytopenia | familial expansibility myocardosis |
| familial polycythemia | Familial hyperlipaemia model | Familial Lipoprotein Badness Xuezheng |
| Familial carry lipoprotein Deficiency disease | familial Motoneuron illness | innocence Familial chronicity pemphigus |
| Familial High Chylomicron Xuezheng | Constitutional familial xanthomatosis | Familial transmissibility cornea denaturalization |
| chronicity Familial granulomatosis | familial local cretinism | Constitutional Familial High cholesterolemia |
| Familial Gaogu Alcoholemia xanthomatosis | Familial Kuangzhou Pigment Exorbitance Aplomb disease | Familial syndrome phenotype |
| Familial High compactness fat Kwashiorkor | Familial hyperlipaemia Hexing | familial Guang'an aciduria Lysinuria disease |
| familial Hypoparathyroidism model | Familial Kuanxue Lipoprotein Overabundance disease | Familial before Lipoprotein cross plethora |
| Familial Cerebella Shiwang webbing angiomatosis | Transmissibility Familial hives syndrome | Non- Familial Dibingzhongqiu Proteinemia disease |
| familial Chromaffinoma illness | Innocence chronicity Familial pemphigus | Acholuria character Familial icterus |
| Idiopathic Non- Familial dystonia | chronicity Familial Non- hemolytic jaundice | Familial transmissibility amyloid degeneration |
| Familial idiopathic dystonia | familial Hypoparathyroidism disease | Myotonia Sexual cycle character Familial anaesthetize |
| High calcemia Digainiaoxing familial | Familial Throb Forelimb abnormal syndrome | Familial fat White deficiency character disease |
| familial Freedom bundle dysfunction | Bielschowsky's-Jansky disease | Familial Male Leave 2 character abnormal syndrome |
| Familial Olfactory nerve Character abort syndrome | Familial addicted to Red blood Reticulocyte Concrescence disease | familial Biniao generate Daohe'er abnormal syndrome |
| Familial Paroxysm nature Muscular tone Deficiencky character Dance athetosis | Familial Paroxysm nature campaign Causality dance athetosis | Familial Amylum appearance Duofaxing Neuropathy become |
| Familial Leak nature Vitreous body cone pathological change | familial Adenoma of colon With multiple Benignant syndrome | Familial Gonad Action Lowness companion Gynaecomastia syndrome |
| familial Gynaecomastia syndrome | Familial Paramyoclonus Cerebella character Dystaxia deafness syndrome | Premature character Familial Cerebella denaturalization syndrome |
| Familial reticulation Endothelial cell Concrescence Zhengban Oxyphil pleocytosis | Procrastination character Familial limitation Heat hives | Familial Pursue Xingbasu Exorbitance Aplomb disease |
| Lethality Familial Gannei Bile gloomy syndrome | Conception Merger Familial polycythemia | familial Erythrophage character reticulocytosis |
| Familial Hormone Generate Barrier character goiter | Familial Dextroglucose galactose malabsorption | Familial Atypia Xingduofazhi melanoma |
| familial Congenital alopecia Diandian Retardation reach | Familial Adenomatosis or Transmissibility polyposis | Familial paramyoclonus Cerebellar ataxia Deafness to sum up |
| Familial Paramyoclonus Cerebella character Dystaxia deafness | Familial Bark cartilage cornea malnutrition synthesis | Jiaxing Myopathy Familial ridge Amyotrophia syndrome |
| Familial Article wind Cholestasia Ganshen synthesis | Familial Bark cartilage cornea malnutrition | Familial White Mucosa plica dysphasia |
| Familial Mucosa White Gauffer character dysphasia | Familial Rosacea Yangzhenban Coat inside epithelioma | Familial Zaoxing Face bark dysphasia |
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