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Mcleod Syndrome
McLeod syndrome
Overview
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Related in the Kosmos
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Syndromes
Alport syndrome
Lelis syndrome
Androgen insensitivity syndrome
22q11.2 deletion syndrome
Syndrome
Hematology
Kell blood group
Red blood cells
Hemolysis
Genetic disorders
(22)
Glycogen storage disease type iib
MASA syndrome
X-linked sideroblastic anemia
Becker's muscular dystrophy
Lipid storage disorder
Lipid storage disorder
Simpson-Go- labi-Behmel syndrome
Aicardi syndrome
Pyruvate dehydrogenase deficiency
Chorea acanthocytosis
Adrenoleuk- odystrophy
Barth syndrome
Kennedy disease
Adenosine deaminase deficiency
X-linked dominant
Dyskeratosis congenita
Wiskott-aldrich syndrome
Chronic granulomatous disease
Haemophilia
Alport syndrome
Lelis syndrome
Androgen insensitivity syndrome
22q11.2 deletion syndrome
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Inborn errors of metabolism
X-linked ichthyosis
Menkes syndrome
Glycogen storage disease type iib
Lipid storage disorder
Adenosine deaminase deficiency
Rare diseases
(8)
Glycogen storage disease type iib
Lipid storage disorder
Chorea acanthocytosis
Lelis syndrome
Menkes syndrome
Menkes syndrome
Adenosine deaminase deficiency
Dyskeratosis congenita
Wiskott-aldrich syndrome
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Autosomal recessive disorders
Glycogen storage disease type iib
Lipid storage disorder
Chorea acanthocytosis
Adenosine deaminase deficiency
Genodermatoses
Focal dermal hypoplasia
Hypohidrotic ectodermal dysplasia
CHILD syndrome
Incontinentia pigmenti
Lelis syndrome
X-linked ichthyosis
Dyskeratosis congenita
Noninfectious immunodeficiency-related cutaneous conditions
(26)
X-linked lymphoproliferative disease
22q11.2 deletion syndrome
Bare lymphocyte syndrome
Cartilage–hair hypoplasia
Chediak–Higashi syndrome
Chediak–Higashi syndrome
Chronic granulomatous disease
Common variable immunodeficiency
Complement deficiency
Graft-versus-host disease
Griscelli syndrome
Hyperimmunoglobulin E syndrome
Immunodeficiency with hyper-immu- noglobulin M
Immunoglobulin M deficiency
Leukocyte adhesion molecule deficiency
Myeloperoxidase deficiency
Neutropenia
Nezelof syndrome
Omenn syndrome
Purine nucleoside phosphorylase deficiency
Selective immunoglobulin A deficiency
Severe combined immunodeficiency
Thymoma with immunodeficiency
WHIM syndrome
Wiskott-aldrich syndrome
X-linked agammaglobulinemia
X-linked hyper-immu- noglobulin M syndrome
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Pulmonology
Organizing pneumonia
Bronchiolitis obliterans
Dyspnea
Genetics
X linked
X-linked recessive
Mutations
Kell antigen system
Diseases and disorders
(31)
Neuroacanthocytosis
X-linked hypophosphatemia
Obstructive lung disease
Centronuclear myopathy
Alveolar soft part sarcoma
Alveolar soft part sarcoma
Glycogen storage disease type iib
MASA syndrome
X-linked sideroblastic anemia
Becker's muscular dystrophy
Lipid storage disorder
Pyruvate dehydrogenase deficiency
Chorea acanthocytosis
Focal dermal hypoplasia
Alport syndrome
X-linked lymphoproliferative disease
Barth syndrome
Androgen insensitivity syndrome
X-linked ichthyosis
Organizing pneumonia
Menkes syndrome
Hypohidrotic ectodermal dysplasia
Kennedy disease
Adenosine deaminase deficiency
22q11.2 deletion syndrome
Bronchiolitis obliterans
CHILD syndrome
Incontinentia pigmenti
Dyskeratosis congenita
Wiskott-aldrich syndrome
Chronic granulomatous disease
Haemophilia
more...
See also
(20)
Hyper IgM Syndrome Type 1
XK protein
Membrane transport protein
Acanthocytes
KAL1
KAL1
Heart-lung transplantation
Allogeneic bone marrow transplantation
Hematological malignancy
Autosomal dominant
Bronchioles
PMID
Colin Munro MacLeod
Phenotype
Carbohydrate metabolism
Unilateral
Congenital malformations
Integument
Complication (medicine)
Diffusion
Immune disorders
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