| Diseases |
Alias |
|
| Mirage Syndrome |
|
Myelodysplasia, Infection, Restriction Of Growth, Adrenal Hypoplasia, Genital Phenotypes, And Enteropathy
|
MIRAGE
|
|
Myelodysplasia, Infection, Restriction Of Growth, Adrenal Hypoplasia, Genital Phenotypes, Enteropathy
|
Myelodysplasia-Infection-Restriction Of Growth-Adrenal Hypoplasia-Genital Anomalies-Enteropathy Syndrome
|
|
Myelodysplasia-Infection-Restriction Of Growth-Adrenal Hypoplasia-Genital Phenotypes-Enteropathy Syndrome
|
Bone Marrow Diseases
|
|
|
| Tumoral Calcinosis, Normophosphatemic, Familial |
|
Normophosphatemic Familial Tumoral Calcinosis
|
NFTC
|
|
Tumoral Calcinosis, Familial, Normophosphatemic
|
Calcinosis, Tumoral, With Normophosphatemia
|
|
Familial Normophosphatemic Tumoral Calcinosis
|
Tumoral Calcinosis With Normophosphatemia
|
|
|
| Monosomy 7 Myelodysplasia And Leukemia Syndrome 2 |
|
|
| Calcinosis |
|
Pathologic Calcification
|
Pathologically Calcified Structure
|
|
|
| Fibromatosis |
|
|
| Pancytopenia |
|
|
| Myelodysplastic Syndrome |
|
Myelodysplastic Syndromes
|
Myelodysplasia
|
|
MDS
|
Myelodysplastic Syndrome Included
|
|
Myelodysplastic Syndrome, Susceptibility To, Included
|
Myelodysplastic Syndrome, Somatic
|
|
Myelodysplastic Syndrome, Susceptibility To
|
|
|
| Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, And Genital Anomalies |
|
Image Syndrome
|
IMAGE
|
|
Intrauterine Growth Retardation-Metaphyseal Dysplasia-Adrenal Hypoplasia Congenita-Genital Anomalies Syndrome
|
Intrauterine Growth Restriction, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, And Genital Anomalies
|
|
Intrauterine Growth Restriction, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, Genital Abnormalities
|
Intrauterine Growth Restriction, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, Genital Anomalies
|
|
Image Anomaly
|
Image Association
|
|
Fetal Growth Retardation
|
Pyle Metaphyseal Dysplasia
|
|
|
| Tumoral Calcinosis, Hyperphosphatemic, Familial, 1 |
|
Hyperphosphatemic Familial Tumoral Calcinosis
|
Hftc
|
|
Hyperostosis-Hyperphosphatemia Syndrome
|
Familial Hyperphosphatemic Tumoral Calcinosis/Hyperphosphatemic Hyperostosis Syndrome
|
|
Tumoral Calcinosis, Hyperphosphatemic, Familial
|
Phptc
|
|
Lipocalcinogranulomatosis
|
Morbus Teutschlaender
|
|
Hhs
|
Hyperostosis With Hyperphosphatemia
|
|
Cortical Hyperostosis With Hyperphosphatemia
|
Primary Hyperphosphatemic Tumoral Calcinosis
|
|
Familial Tumoral Calcinosis
|
HFTC1
|
|
Hypercalcemic Tumoral Calcinosis
|
Hyperphosphatemia Hyperostosis
|
|
Hyperphosphatemia Hyperostosis Syndrome
|
Hyperphosphatemia Tumoral Calcinosis
|
|
Tumoral Calcinosis
|
Calcinosis, Tumoral, With Hyperphosphatemia
|
|
Tumoral Calcinosis, Primary Hyperphosphatemic
|
Teutschlaender Disease, Familial
|
|
Familial Teutschlaender Disease
|
Tumoral Calcinosis With Hyperphosphatemia
|
|
Familial Tumoral Calcinosis/Hyperostosis-Hyperphosphatemia Syndrome
|
Ftc/Hhs
|
|
Familial Tumoral Calcinosis With Hyperphosphatemia
|
Teutschlaender Disease
|
|
Tumoral Calcinosis Primary Hyperphosphatemic
|
Calcinosis, Tumoral, Hyperphosphatemic, Familial
|
|
|
| Immunodeficiency 21 |
|
Monocytopenia And Mycobacterial Infection Syndrome
|
Monomac
|
|
Gata2 Deficiency
|
Monocytopenia With Susceptibility To Infections
|
|
Dcml
|
IMD21
|
|
Dendritic Cell, Monocyte, B Lymphocyte, And Natural Killer Lymphocyte Deficiency
|
Monocytopenia With Susceptibility To Mycobacterial, Fungal, And Papillomavirus Infections And Myelodysplasia
|
|
Combined Immunodeficiency With Susceptibility To Mycobacterial, Viral, And Fungal Infections
|
Combined Immunodeficiency With Susceptibility To Mycobacterial, Viral And Fungal Infections
|
|
Dendritic Cell, Monocyte, B And Nk Lymphoid Deficiency
|
Monocyte-B-Natural Killer-Dendritic Cell Deficiency Syndrome
|
|
Monocytopenia With Mycobacterial, Fungal, And Papillomavirus Infections And Myelodysplasia
|
Combined Immunodeficiency With Mycobacterial, Viral, And Fungal Infections
|
|
Monocyte - B - Natural Killer - Dendritic Cell Deficiency
|
Combined Immunodeficiency With Susceptibility To Mycobacterial Viral And Fungal Infections
|
|
Dendritic Cell Monocyte Lymphocyte B And Natural Killer Lymphocyte Deficiency
|
Monocytopenia With Susceptibility To Mycobacterial Fungal And Papillomavirus Infections And Myelodysplasia
|
|
|
| Diaphyseal Medullary Stenosis With Malignant Fibrous Histiocytoma |
|
DMSMFH
|
Bone Dysplasia With Medullary Fibrosarcoma
|
|
Bdmf
|
Bone Dysplasia With Malignant Fibrous Histiocytoma
|
|
Hardcastle Syndrome
|
Diaphyseal Medullary Stenosis-Bone Malignancy Syndrome
|
|
Myopathy, Limb-Girdle, With Bone Fragility
|
Bone Dysplasia-Medullary Fibrosarcoma Syndrome
|
|
Diaphyseal Medullary Stenosis-Malignant Fibrous Histiocytoma Syndrome
|
Dms-Mfh
|
|
Limb-Girdle Myopathy With Bone Fragility
|
Stenosis, Medullary, Diaphyseal, With Malignant Fibrous Histiocytoma
|
|
|
| Adrenal Hypoplasia, Congenital |
|
X-Linked Adrenal Hypoplasia Congenita
|
Congenital Adrenal Hypoplasia
|
|
AHC
|
Adrenal Hypoplasia, Congenital, With Hypogonadotropic Hypogonadism
|
|
Adrenal Hypoplasia Congenita
|
X-Linked Ahc
|
|
Ahch
|
Ahx
|
|
Ahc With Hhg
|
Cytomegalic Adrenocortical Hypoplasia
|
|
Ahc With Isolated Gonadotropin Deficiency
|
X-Linked Congenital Adrenal Hypoplasia
|
|
Congenital Adrenal Hypoplasia, X-Linked
|
Addison Disease, X-Linked
|
|
Primary Adrenal Hypoplasia
|
Adrenal Hypoplasia Congenital, X-Linked
|
|
X-Linked Addison Disease
|
X-Linked Adrenal Hypoplasia Congenital
|
|
Congenital Hypoplasia Of Adrenal Gland
|
Congenital Adrenal Gland Hypoplasia
|
|
Congenital Small Adrenal Gland
|
Adrenal Hypoplasia
|
|
Cah - [Congenital Adrenal Hypoplasia]
|
|
|
| Adrenal Insufficiency, Congenital, With 46,Xy Sex Reversal, Partial Or Complete |
|
P450scc Deficiency
|
Congenital Adrenal Insufficiency
|
|
Adrenal Insufficiency, Congenital, With 46xy Sex Reversal, Partial Or Complete
|
46,Xy Disorder Of Sex Development-Adrenal Insufficiency Due To Cyp11a1 Deficiency
|
|
Xy Sex Reversal-Adrenal Failure
|
Adrenal Insufficiency, Congenital, With 46,Xy Sex Reversal
|
|
AICSR
|
Adrenal Insufficiency Congenital With 46,Xy Sex Reversal Partial Or Complete
|
|
Adrenal Insufficiency, Congenital
|
Congenital Adrenal Hyperplasia
|
|
Adrenogenital Syndrome
|
|
|
| Familial Glucocorticoid Deficiency |
|
Glucocorticoid Deficiency
|
Acth Resistance
|
|
Adrenal Unresponsiveness To Acth
|
Hereditary Unresponsiveness To Adrenocorticotropic Hormone
|
|
Isolated Glucocorticoid Deficiency
|
Glucocorticoid Deficiency, Familial
|
|
Glucocorticoid Deficiency 1
|
|
|
| Metaphyseal Dysplasia |
|
Bakwin-Krida Syndrome
|
Pyle'S Disease
|
|
Pyle-Cohn Syndrome
|
|
|
| Shwachman-Diamond Syndrome 1 |
|
Shwachman-Diamond Syndrome
|
Shwachman Syndrome
|
|
Shwachman-Bodian-Diamond Syndrome
|
Sds
|
|
Pancreatic Insufficiency And Bone Marrow Dysfunction
|
Shwachman-Bodian Syndrome
|
|
SDS1
|
Lipomatosis Of Pancreas, Congenital
|
|
Congenital Lipomatosis Of Pancreas
|
Shwachman-Diamond Type Metaphyseal Dysplasia
|
|
Metaphyseal Chondrodysplasia, Shwachman Type
|
Shwachman-Diamond-Oski Syndrome
|
|
|
| Achalasia-Addisonianism-Alacrima Syndrome |
|
Allgrove Syndrome
|
Triple-A Syndrome
|
|
Achalasia-Addisonianism-Alacrimia Syndrome
|
Alacrima-Achalasia-Adrenal Insufficiency Neurologic Disorder
|
|
Triple A Syndrome
|
Aaa Syndrome
|
|
AAAS
|
Glucocorticoid Deficiency With Achalasia
|
|
Glucocorticoid Deficiency And Achalasia
|
Addisonian-Achalasia Syndrome
|
|
Hypoadrenalism With Achalasia
|
Alacrima-Achalasia-Addisonianism
|
|
Aaa
|
Acth-Resistant Adrenal Insufficiency, Achalasia And Alacrima
|
|
Achalasia Addisonianism Alacrimia Syndrome
|
Achalasia Alacrima Syndrome
|
|
Addisonian Achalasia Syndrome
|
Achalasia-Addisonian Syndrome
|
|
Achalasia-Alacrima Syndrome
|
2a Syndrome
|
|
3a Syndrome
|
4a Syndrome
|
|
Adrenal Insufficiency-Achalasia-Alacrima Syndrome
|
Double A Syndrome
|
|
Quaternary A Syndrome
|
Acth-Resistant Adrenal Insufficiency With Achalasia And Alacrima
|
|
Allgrove'S Syndrome
|
Adrenal Gland Hypofunction
|
|
Adrenal Cortical Hypofunction
|
|
|
| Amegakaryocytic Thrombocytopenia, Congenital |
|
Congenital Amegakaryocytic Thrombocytopenia
|
CAMT
|
|
Thrombocytopenia, Congenital Amegakaryocytic
|
Congenital Amegakaryocytic Thrombocytopenic Purpura
|
|
Thrombocytopenia Congenital Amegakaryocytic
|
Thrombocytopenia, Amegakaryocytic, Congenital
|
|
|
| Osteogenesis Imperfecta, Type Ii |
|
Vrolik Type Of Osteogenesis Imperfecta
|
Osteogenesis Imperfecta Type 2
|
|
OI2
|
Oi, Type Ii
|
|
Osteogenesis Imperfecta Congenita
|
Oic
|
|
Osteogenesis Imperfecta Type Ii
|
Lethal Osteogenesis Imperfecta
|
|
Oi Type 2
|
Osteogenesis Imperfecta Congenita Perinatal Lethal Form
|
|
Osteogenesis Imperfecta Congenita, Perinatal Lethal Form
|
Perinatal Lethal Osteogenesis Imperfecta Congenita
|
|
Perinatally Lethal Oi
|
Osteogenesis Imperfecta 2
|
|
Oi-Ii
|
Oi-Iia
|
|
Oi Type Iia
|
Osteogenesis Imperfecta Type Iia
|
|
Osteogenesis Imperfecta Type Ii Autosomal Dominant
|
Oi Type Ii
|
|
Osteogenesis Imperfecta, Dominant Perinatal Lethal
|
|
|
| Juvenile Myelomonocytic Leukemia |
|
Leukemia, Juvenile Myelomonocytic
|
JMML
|
|
Leukemia, Juvenile Myelomonocytic, Somatic
|
Juvenile Chronic Myelomonocytic Leukemia
|
|
Juvenile Chronic Myelogenous Leukemia
|
Leukemia, Myelomonocytic, Juvenile
|
|
Juvenile Myelomonocytic Leukaemia Without Mention Of Remission
|
|
|
| Severe Congenital Neutropenia |
|
Congenital Neutropenia
|
Neutropenia, Severe Congenital
|
|
Congenital Agranulocytosis
|
Infantile Genetic Agranulocytosis
|
|
Kostmann Disease
|
Kostmann'S Agranulocytosis
|
|
Kostmann'S Syndrome
|
Severe Infantile Genetic Neutropenia
|
|
|
| Dyskeratosis Congenita |
|
Dyskeratosis Congenita Autosomal Dominant
|
Dc
|
|
Dkc
|
Zinsser-Engman-Cole Syndrome
|
|
Dyskeratosis Congenita, Autosomal Dominant
|
Autosomal Dominant Dyskeratosis Congenita
|
|
Dkca
|
Dyskeratosis Congenita Scoggins Type
|
|
Zinsser-Cole-Engman Syndrome
|
X-Linked Dyskeratosis Congenita
|
|
Hoyeraal-Hreidarsson Syndrome
|
|
|
| Diamond-Blackfan Anemia |
|
Congenital Pure Red Cell Aplasia
|
Aase Syndrome
|
|
Erythrogenesis Imperfecta
|
Anemia, Diamond-Blackfan
|
|
Congenital Hypoplastic Anemia
|
Aase-Smith Ii Syndrome
|
|
Bds
|
Blackfan-Diamond Anemia
|
|
Congenital Prca
|
Congenital Hypoplastic Anemia, Blackfan-Diamond Type
|
|
Dba
|
Blackfan - Diamond Syndrome
|
|
Chronic Constitutional Pure Red Cell Anaemia
|
Anemia Diamond Blackfan Type
|
|
Anemia Congenital Erythroid Hypoplastic
|
Aregenerative Anemia Chronic Congenital
|
|
Blackfan Diamond Syndrome
|
Red Cell Aplasia, Pure Hereditary
|
|
Aase-Smith Syndrome Ii
|
Bda
|
|
Blackfan Diamond Anemia
|
Blackfan-Diamond Disease
|
|
Blackfan-Diamond Syndrome
|
Chronic Congenital Agenerative Anemia
|
|
Congenital Erythroid Hypoplastic Anemia
|
Congenital Hypoplastic Anemia Of Blackfan And Diamond
|
|
Congenital Pure Red Cell Anemia
|
Hypoplastic Congenital Anemia
|
|
Inherited Erythroblastopenia
|
Pure Hereditary Red Cell Aplasia
|
|
Anemia, Hypoplastic, Congenital
|
Anemia Hypoplastic Congenital
|
|
Fanconi Anemia
|
Constitutional Aplastic Anemia
|
|
Diamond-Blackfan Anemia 1
|
Aase Smith Syndrome 2
|
|
Congenital Red Cell Aplasia
|
Red Cell Aplasia Of Infants
|
|
Pure Red Cell Aplasia Of Infants
|
Congenital Red Cell Aplastic Anaemia
|
|
Congenital Pure Red Cell Anaemia
|
Congenital Erythroid Hypoplasia
|
|
Pearson Marrow-Pancreas Syndrome
|
|
|
