1 (90.1%)
|
hereditary spherocytosis type 4
|
Hemolytic anemia
Hyperbilirubinemia
Jaundice
Spherocytosis
Splenomegaly
Autosomal dominant inheritance
Any hereditary spherocytosis in which the cause of the disease is a mutation in the SLC4A1 gene.
OMIM:612653
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Monarch
GTR:C2675212
|
1 (90.1%)
|
hereditary spherocytosis type 2
|
Hemolytic anemia
Hyperbilirubinemia
Jaundice
Spherocytosis
Splenomegaly
Autosomal dominant inheritance
Any hereditary spherocytosis in which the cause of the disease is a mutation in the SPTB gene.
OMIM:616649
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Monarch
GTR:C2674219
|
1 (90.1%)
|
hereditary spherocytosis type 1
|
Hemolytic anemia
Hyperbilirubinemia
Jaundice
Spherocytosis
Splenomegaly
Autosomal dominant inheritance
Autosomal recessive inheritance
Any hereditary spherocytosis in which the cause of the disease is a mutation in the ANK1 gene.
OMIM:182900
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Monarch
KEGG:H00230
GTR:C2674218
|
4 (87.7%)
|
overhydrated hereditary stomatocytosis
|
Hemolytic anemia
Hyperbilirubinemia
Jaundice
Splenomegaly
Stomatocytosis
Autosomal dominant inheritance
Overhydrated hereditary stomatocytosis (OHSt) is a disorder of red cell membrane permeability to monovalent cations and is characterized clinically by hemolytic anemia.
OMIM:185000
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Monarch
KEGG:H00232
KEGG:H01979
GTR:C1861455
|
4 (87.7%)
|
dehydrated hereditary stomatocytosis 2
|
Acanthocytosis
Hemolytic anemia
Hyperbilirubinemia
Jaundice
Splenomegaly
Autosomal dominant inheritance
Any dehydrated hereditary stomatocytosis in which the cause of the disease is a mutation in the KCNN4 gene.
OMIM:616689
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Monarch
GTR:C4225242
|
4 (87.7%)
|
anemia, congenital dyserythropoietic, type 1a
|
Hydrops fetalis
Macrocytic dyserythropoietic anemia
Poikilocytosis
Prolonged neonatal jaundice
Splenomegaly
Autosomal recessive inheritance
OMIM:224120
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Monarch
KEGG:H00917
Gene Reviews
|
4 (87.7%)
|
anemia, nonspherocytic hemolytic, due to G6PD deficiency
|
Fava bean-induced hemolytic anemia
Fever
Poikilocytosis
Prolonged neonatal jaundice
Splenomegaly
X-linked recessive inheritance
X-linked dominant inheritance
OMIM:300908
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Monarch
KEGG:H00668
KEGG:H01375
GTR:C2720289
|
8 (85.6%)
|
elliptocytosis 1
|
Elliptocytosis
Hemolytic anemia
Jaundice
Splenomegaly
Autosomal dominant inheritance
Autosomal recessive inheritance
Any hereditary elliptocytosis in which the cause of the disease is a mutation in the EPB41 gene.
OMIM:611804
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Monarch
KEGG:H00231
GTR:C2678497
|
8 (85.6%)
|
congenital dyserythropoietic anemia type type 1B
|
Anemia of inadequate production
Jaundice
Poikilocytosis
Splenomegaly
Autosomal recessive inheritance
OMIM:615631
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Monarch
Gene Reviews
GTR:C3810185
|
10 (82.9%)
|
lathosterolosis
|
Acanthocytosis
Hepatosplenomegaly
Hyperbilirubinemia
Intrahepatic cholestasis
Autosomal recessive inheritance
Lathosterolosis is an extremely rare inborn error of sterol biosynthesis characterized by facial dysmorphism, congenital anomalies (including limb and kidney anomalies), failure to thrive, developmental delay and liver disease.
OMIM:607330
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Monarch
KEGG:H01281
GTR:C1846421
|
11 (80.6%)
|
Bernard-Soulier syndrome, type A2, autosomal dominant
|
Hemolytic anemia
Menorrhagia
Petechiae
Splenomegaly
Stomatocytosis
Autosomal dominant inheritance
A Bernard-Soulier syndrome characterized by autosomal dominant inheritance of mild to moderate bleeding tendency, thrombocytopenia, and an increased mean platelet size that has material basis in heterozygous mutations in the GP1BA gene on chromosome 17p.
OMIM:153670
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Monarch
KEGG:H00224
GTR:C3277076
|
12 (80.2%)
|
cystic fibrosis-gastritis-megaloblastic anemia syndrome
|
Biliary cirrhosis
Exocrine pancreatic insufficiency
Megaloblastic anemia
Reduced blood folate concentration
Autosomal recessive inheritance
A rare genetic disease reported in two siblings of consanguineous Arab parents and is characterized by cystic fibrosis, gastritis associated with Helicobacter pylori, folate deficiency megaloblastic anemia, and intellectual disability. There have been no further descriptions in the literature since 1991.
OMIM:219721
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Monarch
|
13 (80.2%)
|
severe congenital hypochromic anemia with ringed sideroblasts
|
Anemia
Hepatomegaly
Increased circulating ferritin concentration
Poikilocytosis
Splenomegaly
Autosomal dominant inheritance
STEAP3/TSAP6-related sideroblastic anemia is a very rare severe non-syndromic hypochromic anemia, which is characterized by transfusion-dependent hypochromic, poorly regenerative anemia, iron overload, resembling non-syndromic sideroblastic anemia except for increased erythrocyte protoporphyrin levels.
OMIM:615234
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Monarch
GTR:C3808920
GTR:C4511137
|
13 (80.2%)
|
sitosterolemia 1
|
Abnormality of the liver
Episodic hemolytic anemia
Hypercholesterolemia
Splenomegaly
Stomatocytosis
Autosomal recessive inheritance
OMIM:210250
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Monarch
KEGG:H00152
Gene Reviews
GTR:C0342907
|
15 (78.9%)
|
cryohydrocytosis
|
Abnormality of metabolism/homeostasis
Hemolytic anemia
Splenomegaly
Stomatocytosis
Autosomal dominant inheritance
A rare, hereditary, hemolytic anemia due to a red cell membrane anomaly characterized by fatigue, mild anemia and pseudohyperkalemia due to a potassium leak from the red blood cells. A hallmark of this condition is that red blood cells lyse on storage at 4 degrees centigrade.
OMIM:185020
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Monarch
KEGG:H02002
GTR:C1861453
|
16 (78.4%)
|
anemia, nonspherocytic hemolytic, possibly due to defect in porphyrin metabolism
|
Elevated urinary delta-aminolevulinic acid
Jaundice
Nonspherocytic hemolytic anemia
Splenomegaly
Autosomal recessive inheritance
OMIM:206400
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Monarch
GTR:C1859785
|
16 (78.4%)
|
congenital dyserythropoietic anemia type 2
|
Anemia of inadequate production
Endopolyploidy on chromosome studies of bone marrow
Jaundice
Reticulocytosis
Splenomegaly
Autosomal recessive inheritance
Congenital dyserythropoietic anemia type II (CDA II) is the most common form of CDA characterized by anemia, jaundice and splenomegaly and often leading to liver iron overload and gallstones.
OMIM:224100
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Monarch
|
16 (78.4%)
|
hyperbilirubinemia, shunt, primary
|
Anemia of inadequate production
Hyperbilirubinemia
Jaundice
Reticulocytosis
Splenomegaly
Autosomal dominant inheritance
OMIM:237800
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Monarch
|
16 (78.4%)
|
hemolytic anemia due to diphosphoglycerate mutase deficiency
|
Abnormality of metabolism/homeostasis
Jaundice
Normochromic anemia
Splenomegaly
Autosomal recessive inheritance
A rare, autosomal recessive, inherited disorder caused by mutation of the BPGM gene. It is characterized by hemolytic anemia and splenomegaly.
OMIM:222800
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Monarch
GTR:C1291620
|
16 (78.4%)
|
dehydrated hereditary stomatocytosis with or without pseudohyperkalemia and/or perinatal edema
|
Exercise-induced hemolysis
Increased circulating ferritin concentration
Jaundice
Reticulocytosis
Splenomegaly
Autosomal dominant inheritance
OMIM:194380
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Monarch
KEGG:H01978
KEGG:H02001
|
16 (78.4%)
|
pyruvate kinase deficiency of red cells
|
Chronic hemolytic anemia
Jaundice
Nonimmune hydrops fetalis
Reticulocytosis
Splenomegaly
Autosomal recessive inheritance
Hemolytic anemia due to red cell pyruvate kinase (PK) deficiency is a metabolic disorder characterized by a variable degree of chronic nonspherocytic hemolytic anemia.
OMIM:266200
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Monarch
KEGG:H01096
GTR:C0340968
|
16 (78.4%)
|
non-spherocytic hemolytic anemia due to hexokinase deficiency
|
Abnormality of metabolism/homeostasis
Jaundice
Normochromic anemia
Splenomegaly
Autosomal recessive inheritance
Nonspherocytic hemolytic anemia due to hexokinase deficiency (NSHA due to HK1 deficiency) is a very rare conditionmainly characterized by severe, chronic hemolysis, beginning in infancy. Approximately 20 cases of this condition have been described to date. Signs and symptoms of hexokinase deficiency are very similar to those of pyruvate kinase deficiency but anemia is generally more severe. Some affected individuals reportedly have had various abnormalities in addition to NSHA including multiple malformations, panmyelopathy, and latent diabetes.Itcan be caused by mutations in the HK1 gene and is inherited in an autosomal recessive manner. Treatment may include red cell transfusions for those with severe anemia.
OMIM:235700
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Monarch
KEGG:H00664
|
16 (78.4%)
|
sideroblastic anemia 3
|
Anemia
Conjugated hyperbilirubinemia
Jaundice
Splenomegaly
Autosomal recessive inheritance
OMIM:616860
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Monarch
|
16 (78.4%)
|
hemolytic anemia due to glucophosphate isomerase deficiency
|
Decreased glucosephosphate isomerase level
Jaundice
Nonspherocytic hemolytic anemia
Splenomegaly
Autosomal recessive inheritance
Glucosephosphate isomerase (GPI) deficiency is an erythroenzymopathy characterized by chronic nonspherocytic hemolytic anemia.
OMIM:613470
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Monarch
GTR:C3150730
GTR:CN072763
|
16 (78.4%)
|
sickle cell anemia
|
Hematuria
Hemolytic anemia
Jaundice
Splenomegaly
Autosomal recessive inheritance
Sickle cell anemias are chronic hemolytic diseases that may induce three types of acute accidents: severe anemia, severe bacterial infections, and ischemic vasoocclusive accidents (VOA) caused by sickle-shaped red blood cells obstructing small blood vessels and capillaries. Many diverse complications can occur.
OMIM:603903
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Monarch
KEGG:H00229
Gene Reviews
GTR:C0002895
|
16 (78.4%)
|
hereditary cryohydrocytosis with reduced stomatin
|
Hemolytic anemia
Hyperkalemia
Jaundice
Splenomegaly
Autosomal dominant inheritance
OMIM:608885
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Monarch
GTR:C1837206
|
16 (78.4%)
|
hereditary coproporphyria
|
Abnormality of metabolism/homeostasis
Congenital hemolytic anemia
Jaundice
Splenomegaly
Autosomal dominant inheritance
Autosomal recessive inheritance
Hereditary coproporphyria is a form of acute hepatic porphyria characterized by the occurrence of neuro-visceral attacks and, more rarely, by the presence of cutaneous lesions.
OMIM:121300
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Monarch
Gene Reviews
GTR:C0162531
|
16 (78.4%)
|
prolidase deficiency
|
Abnormality of metabolism/homeostasis
Anemia
Prolonged neonatal jaundice
Splenomegaly
Autosomal recessive inheritance
Prolidase deficiency is an inherited disorder of peptide metabolism characterized by severe skin lesions, recurrent infections (involving mainly the skin and respiratory system), dysmorphic facial features, variable cognitive impairment, and splenomegaly.
OMIM:170100
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Monarch
KEGG:H01119
Gene Reviews
GTR:C0268532
|
16 (78.4%)
|
familial hemophagocytic lymphohistiocytosis type 1
|
Anemia
Hypertriglyceridemia
Jaundice
Splenomegaly
Autosomal recessive inheritance
Familial Hemophagocytic lymphohistiocytosis (FHL) is a rare primary immunodeficiency characterized by a macrophage activation syndrome with an onset usually occurring within a few months or less common several years after birth.
OMIM:267700
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Monarch
Gene Reviews
GTR:C0272199
GTR:CN034020
GTR:CN205265
|
16 (78.4%)
|
familial hemophagocytic lymphohistiocytosis 2
|
Anemia
Hypertriglyceridemia
Jaundice
Splenomegaly
Autosomal recessive inheritance
Any genetic hemophagocytic lymphohistiocytosis in which the cause of the disease is a mutation in the PRF1 gene.
OMIM:603553
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Monarch
KEGG:H00109
Gene Reviews
|
31 (77.5%)
|
celiac disease, susceptibility to, 1
|
Elevated hepatic transaminase
Iron deficiency anemia
Reduced blood folate concentration
Autosomal recessive inheritance
Heterogeneous
Multifactorial inheritance
OMIM:212750
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Monarch
KEGG:H02123
Gene Reviews
|
32 (77.5%)
|
red cell phospholipid defect with hemolysis
|
Hyperbilirubinemia
Intermittent jaundice
Reticulocytosis
Splenomegaly
Autosomal dominant inheritance
OMIM:179700
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Monarch
GTR:C1867339
|
33 (76.8%)
|
thrombocytopenia, anemia, and myelofibrosis
|
Anemia
Anisopoikilocytosis
Splenomegaly
Autosomal recessive inheritance
OMIM:617441
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Monarch
GTR:C4479504
|
34 (76.6%)
|
McLeod neuroacanthocytosis syndrome
|
Acanthocytosis
Elevated serum creatine kinase
Hepatosplenomegaly
X-linked inheritance
McLeod neuroacanthocytosis syndrome (MLS) is a form of neuroacanthocytosis and is characterized clinically by a Huntington's disease-like phenotype with an involuntary hyperkinetic movement disorder, psychiatric manifestations and cognitive alterations, and biochemically by absence of the Kx antigen and by weak expression of the Kell antigens.
OMIM:300842
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Monarch
KEGG:H00655
Gene Reviews
|
35 (76.3%)
|
congenital bile acid synthesis defect 5
|
Iron deficiency anemia
Jaundice
Splenomegaly
Autosomal recessive inheritance
Any congenital bile acid synthesis defect in which the cause of the disease is a mutation in the ABCD3 gene.
OMIM:616278
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Monarch
|
35 (76.3%)
|
glycogen storage disease due to aldolase A deficiency
|
Epicanthus
Jaundice
Normochromic anemia
Splenomegaly
Autosomal recessive inheritance
Glycogen storage disease due to aldolase A deficiency is an extremely rare glycogen storage disease characterized by hemolytic anemia with or without myopathy or intellectual deficit. Myopathy can be severe enough to result in fatal rhabdomyolysis in some patients. A family with episodic rhabdomyolysis (triggerd by fever) without hemolytic anemia has recently been reported.
OMIM:611881
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Monarch
KEGG:H01952
GTR:C0272066
|
35 (76.3%)
|
pancreatic insufficiency-anemia-hyperostosis syndrome
|
Anemia
Carious teeth
Jaundice
Splenomegaly
Autosomal recessive inheritance
This syndrome is characterized by exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis.
OMIM:612714
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Monarch
KEGG:H00920
GTR:C2675184
GTR:C4302747
|
35 (76.3%)
|
triosephosphate isomerase deficiency
|
Jaundice
Normochromic anemia
Optic disc pallor
Splenomegaly
Autosomal recessive inheritance
Triosephosphate isomerase (TPI) deficiency is a severe autosomal recessive inherited multisystem disorder of glycolytic metabolism characterized by hemolytic anemia and neurodegeneration.
OMIM:615512
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Monarch
GTR:C1860808
|
35 (76.3%)
|
Niemann-Pick disease type A
|
Microcytic anemia
Osteoporosis
Prolonged neonatal jaundice
Splenomegaly
Autosomal recessive inheritance
Niemann-Pick disease type A is a very severe subtype of Niemann-Pick disease, an autosomal recessive lysosomal disease, and is characterized clinically by onset in infancy or early childhood with failure to thrive, hepatosplenomegaly, and rapidly progressive neurodegenerative disorders.
OMIM:257200
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Monarch
KEGG:H00137
KEGG:H00424
Gene Reviews
GTR:C0268242
|
35 (76.3%)
|
Chediak-Higashi syndrome
|
Anemia
Gingivitis
Jaundice
Splenomegaly
Autosomal recessive inheritance
ChC)diak-Higashi syndrome (CHS) is a rare severe genetic disorder generally characterized by partial oculocutaneous albinism (OCA), severe immunodeficiency, mild bleeding, neurological dysfunction and lymphoproliferative disorder. A classic, early-onset form and an attenuated, later-onset form (Atypical CHS) have been described.
OMIM:214500
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Monarch
KEGG:H00101
KEGG:H02021
Gene Reviews
GTR:C0007965
|
41 (76.2%)
|
Rh deficiency syndrome
|
Hemolytic anemia
Jaundice
Stomatocytosis
Unconjugated hyperbilirubinemia
Autosomal dominant inheritance
The Rh deficiency syndrome, also known as Rh-null syndrome, is a blood disorder where people have red blood cells (RBCs) lacking all Rh antigens. The Rh antigens maintain the integrity of the RBC membrane and therefore, RBCs which lack Rh antigens have an abnormal shape. There are two types of Rh deficiency syndrome: The regulator type is associated with many different changes (mutations) in the RHAG gene. The amorph type is caused by inactive copies of a gene (silent alleles) at the RH locus. As a result, the RBCs do not express any of the Rh antigens. The absence of the Rh complex alters the RBC shape, increases its tendency to break down (osmotic fragility), and shortens its lifespan, resulting in a hemolytic anemia that is usually mild. These patients are at risk of having adverse transfusion reactions because they may produce antibodies against several of the Rh antigens and can only receive blood from people who have the same condition. Rh deficiency syndrome is inherited in an autosomal recessive manner. Management is individualized according to the severity of hemolytic anemia.
OMIM:268150
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Monarch
KEGG:H01214
GTR:C0272052
GTR:C1849387
|
41 (76.2%)
|
congenital thrombotic thrombocytopenic purpura
|
Jaundice
Microangiopathic hemolytic anemia
Proteinuria
Schistocytosis
Autosomal recessive inheritance
Congenital thrombotic thrombocytopenic purpura is the hereditary form of thrombotic thrombocytopenic purpura (TTP) characterized by profound peripheral thrombocytopenia, microangiopathic hemolytic anemia (MAHA) and single or multiple organ failure of variable severity.
OMIM:274150
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Monarch
KEGG:H00225
|
43 (75.6%)
|
letterer-Siwe disease
|
Anemia
Fever
Hepatosplenomegaly
Jaundice
Autosomal recessive inheritance
A multifocal, multisystem form of Langerhans-cell histiocytosis. There is involvement of multiple organ systems including the bones, skin, liver, spleen, and lymph nodes. Patients are usually infants presenting with fever, hepatosplenomegaly, lymphadenopathy, bone and skin lesions, and pancytopenia.
OMIM:246400
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Monarch
GTR:C0023381
|
44 (75.3%)
|
fibrosis, neurodegeneration, and cerebral angiomatosis
|
Chronic hemolytic anemia
Hepatomegaly
Poikilocytosis
Strabismus
Autosomal recessive inheritance
OMIM:618278
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|
45 (74.6%)
|
cutaneous porphyria
|
Cholelithiasis
Hemolytic anemia
Pink urine
Splenomegaly
Autosomal recessive inheritance
Congenital erythropoietic porphyria, or Günther disease, is a form of erythropoietic porphyria characterized by very severe and mutilating photodermatosis.
OMIM:263700
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Monarch
Gene Reviews
|
46 (74.5%)
|
primary familial polycythemia due to EPO receptor mutation
|
Hypertension
Increased red blood cell mass
Plethora
Splenomegaly
Autosomal dominant inheritance
Primary familial polycythemia is an inherited hematological disorder resulting from mutations in the erythropoietin (EPO) receptor and is characterized by an elevated absolute red blood cell mass caused by uncontrolled red blood cell production in the presence of low EPO levels.
OMIM:133100
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Monarch
KEGG:H00236
Gene Reviews
|
47 (73.5%)
|
COG6-CGD
|
Anemia
Cholestasis
Splenomegaly
Type II transferrin isoform profile
Autosomal recessive inheritance
OMIM:614576
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Monarch
GTR:C3553230
|
48 (73.5%)
|
reticuloendotheliosis, X-linked
|
Anemia
Hepatosplenomegaly
Jaundice
X-linked inheritance
OMIM:312500
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Monarch
GTR:C0035288
|
48 (73.5%)
|
cyanosis, transient neonatal
|
Anemia
Hepatomegaly
Jaundice
Autosomal dominant inheritance
OMIM:613977
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Monarch
GTR:C3151421
|
48 (73.5%)
|
constitutional megaloblastic anemia with severe neurologic disease
|
Hepatomegaly
Jaundice
Megaloblastic anemia
Autosomal recessive inheritance
OMIM:613839
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Monarch
KEGG:H01197
|
51 (73.3%)
|
autoimmune lymphoproliferative syndrome type 1
|
Autoimmune hemolytic anemia
Decreased lymphocyte apoptosis
Splenomegaly
Urticaria
Autosomal dominant inheritance
OMIM:601859
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Monarch
KEGG:H00108
Gene Reviews
|
51 (73.3%)
|
autoimmune lymphoproliferative syndrome type 2A
|
Autoimmune hemolytic anemia
Decreased lymphocyte apoptosis
Splenomegaly
Urticaria
Autosomal dominant inheritance
A rare, primary immunodeficiency with an autosomal dominant pattern of inheritance but incomplete penetrance. It is caused by a mutation in the CASP10 (caspase-10) gene that leads to defective Fas-induced apoptosis. Disruption of Fas-induced apoptosis impairs lymphocyte homeostasis and immune tolerance. Characteristic laboratory findings include an increase in circulating, double-negative (CD4-/CD8-) T cells in the setting of immune-mediated anemia, thrombocytopenia and neutropenia. Clinical signs present in childhood include fatigue, pallor, bruising, hepatosplenomegaly and chronic, non-malignant, non-infectious lymphadenopathy. The clinical course is influenced by a strong association with other autoimmune disorders and an increased risk for developing Hodgkin and non-Hodgkin lymphoma.
OMIM:603909
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Monarch
Gene Reviews
GTR:C1519709
GTR:C1858968
|
51 (73.3%)
|
Gaucher disease perinatal lethal
|
Anemia
Nonimmune hydrops fetalis
Petechiae
Splenomegaly
Autosomal recessive inheritance
Fetal Gaucher disease is the perinatal lethal form of Gaucher disease (GD).
OMIM:608013
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Monarch
Gene Reviews
GTR:C1842704
|
51 (73.3%)
|
vasculitis due to ADA2 deficiency
|
Anemia
Cutis marmorata
Fever
Splenomegaly
Autosomal recessive inheritance
Vasculitis due to ADA2 deficiency is a rare, genetic, systemic and rheumatologic disease due to adenosine deaminase-2 inactivating mutations, combining variable features of autoinflammation, vasculitis, and a mild immunodeficiency. Variable clinical presentation includes chronic or recurrent systemic inflammation with fever, livedo reticularis or racemosa, early-onset ischemic or hemorrhagic strokes, peripheral neuropathy, abdominal pain, hepatosplenomegaly, portal hypertension, cutaneous polyarteritis nodosa, variable cytopenia and immunoglobulin deficiency.
OMIM:615688
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Monarch
KEGG:H01382
Gene Reviews
|
51 (73.3%)
|
proteasome-associated autoinflammatory syndrome 1
|
Anemia
Erythema
Hypertriglyceridemia
Splenomegaly
Autosomal recessive inheritance
OMIM:256040
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Monarch
KEGG:H01741
|
56 (72.3%)
|
short-rib thoracic dysplasia 9 with or without polydactyly
|
Anemia
Cholestasis
Hepatomegaly
Nephronophthisis
Autosomal recessive inheritance
An asphyxiating thoracic dystrophy that has material basis in homozygous or compound heterozygous mutation in the IFT140 gene on chromosome 16p13.
OMIM:266920
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Monarch
|
57 (71.5%)
|
ALG8-CDG
|
Abnormal isoelectric focusing of serum transferrin
Anemia
Cholestasis
Hepatomegaly
Autosomal recessive inheritance
A form of congenital disorders of N-linked glycosylation that is characterized by gastrointestinal symptoms (diarrhea, vomiting, feeding problems with failure to thrive, protein-losing enteropathy), edema and ascites (including hydrops fetalis), hepatomegaly, renal tubulopathy, coagulation anomalies due to thrombocytopenia, brain involvement (psychomotor delay, seizures, ataxia), facial dysmorphism (low-set ears and retrognathia), pes equinovarus, and muscular hypotonia. Cataracts may also be observed. Prognosis is usually poor. The disease is caused by loss-of-function mutations in the gene ALG8 (11q14.1), resulting in a block in the initial step of protein glycosylation.
OMIM:608104
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Monarch
Gene Reviews
GTR:C2931002
|
58 (71.2%)
|
beta-thalassemia-X-linked thrombocytopenia syndrome
|
Epistaxis
Hemolytic anemia
Petechiae
Splenomegaly
X-linked recessive inheritance
Beta-thalassemia - X-linked thrombocytopenia is a form of beta-thalassemia characterized by splenomegaly and petechiae, moderate thrombocytopenia, prolonged bleeding time due to platelet dysfunction, reticulocytosis and mild beta-thalassemia.
OMIM:314050
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Monarch
Gene Reviews
GTR:C1839161
|
58 (71.2%)
|
leukocyte adhesion deficiency 3
|
Anemia
Epistaxis
Petechiae
Splenomegaly
Autosomal recessive inheritance
Leukocyte adhesion deficiency type III (LAD-III) is a form of LAD characterized by both severe bacterial infections and a severe bleeding disorder.
OMIM:612840
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Monarch
GTR:C2748536
|
58 (71.2%)
|
transaldolase deficiency
|
Anemia
Splenomegaly
Telangiectasia
Wide mouth
Autosomal recessive inheritance
Transaldolase deficiency is an inborn error of the pentose phosphate pathway that presents in the neonatal or antenatal period with hydrops fetalis, hepatosplenomegaly, hepatic dysfunction, thrombocytopenia, anemia, and renal and cardiac abnormalities.
OMIM:606003
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Monarch
KEGG:H01189
GTR:C1291329
|