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eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine



   ghosal hematodiaphyseal dysplasia
  

Disease ID 1580
Disease ghosal hematodiaphyseal dysplasia
Definition
Ghosal hematodiaphyseal dysplasia is a metabolic disorder. - Wikipedia
Reference: https://en.wikipedia.org/wiki/ghosal hematodiaphyseal dysplasia
Synonym
diaphyseal dysplasia with anaemia
diaphyseal dysplasia with anemia
diaphyseal dysplasia with anemia (disorder)
ghdd
ghosal haematodiaphyseal dysplasia
ghosal syndrome
Orphanet
OMIM
UMLS
C1856465
SNOMED-CT
Curated Gene
Entrez_id | Symbol | Resource(Total Genes:1)
6916  |  TBXAS1  |  CLINVAR;CTD_human;ORPHANET;UNIPROT
Inferring Gene(Waiting for update.)
Text Mined Gene(Waiting for update.)
Locus
Symbol | Locus(Total Locus:1)
TBXAS1  |  7q34
Disease ID 1580
Disease ghosal hematodiaphyseal dysplasia
Integrated Phenotype
HPO | Name(Total Integrated Phenotypes:13)
HP:0001744  |  Splenomegaly
HP:0003312  |  Abnormal form of the vertebral bodies
HP:0006487  |  Bowing of the long bones
HP:0010978  |  Abnormality of immune system physiology
HP:0002167  |  Neurological speech impairment
HP:0001903  |  Anemia
HP:0003103  |  Abnormal cortical bone morphology
HP:0005019  |  Diaphyseal thickening
HP:0002992  |  Abnormality of the tibia
HP:0002644  |  Abnormality of pelvic girdle bone morphology
HP:0004493  |  Craniofacial hyperostosis
HP:0002823  |  Abnormality of the femur
HP:0000944  |  Abnormality of the metaphyses
Text Mined Phenotype(Waiting for update.)
Disease ID 1580
Disease ghosal hematodiaphyseal dysplasia
Manually Symptom(Waiting for update.)
Text Mined Symptom(Waiting for update.)
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
Text Mining Genotype(Total Genotypes:0)
(Waiting for update.)
All Snps(Total Genotypes:1)
snpId pubmedId geneId geneSymbol diseaseId sourceId sentence score Year geneSymbol_dbSNP CHROMOSOME POS REF ALT
rs794727053NA6916TBXAS1umls:C1856465CLINVARNA0.480271442NATBXAS17140017726G-
GWASdb Annotation(Total Genotypes:0)
(Waiting for update.)
GWASdb Snp Trait(Total Genotypes:0)
(Waiting for update.)
Mapped by lexical matching(Total Items:8)
HP ID HP Name MP ID MP Name Annotation
HP:0006487Bowing of the long bonesMP:0013621decreased internal diameter of femurreduced cross-sectional distance that extends from one lateral edge of the femur long bone marrow cavity, through its center and to the opposite lateral edge of the bone marrow cavity through the mid point of the femur
HP:0003103Abnormal cortical bone morphologyMP:0013640increased bone stiffnessincrease in material stiffness (N/mm) during elastic deformation
HP:0002644Abnormality of pelvic girdle bone morphologyMP:0013620increased internal diameter of femurincreased cross-sectional distance that extends from one lateral edge of the femur long bone marrow cavity, through its center and to the opposite lateral edge of the bone marrow cavity through the mid point of the femur
HP:0000944Abnormality of the metaphysesMP:0013621decreased internal diameter of femurreduced cross-sectional distance that extends from one lateral edge of the femur long bone marrow cavity, through its center and to the opposite lateral edge of the bone marrow cavity through the mid point of the femur
HP:0002823Abnormality of the femurMP:0020010decreased bone mineral density of femurreduction in the quatitative measurment value of mineral content of bone in the long bone of the thigh
HP:0002992Abnormality of the tibiaMP:0012528abnormal zone of polarizing activity morphologyany structural anomaly of the subset of cells found in the posterior mesenchyme region of the vertebrate limb bud; Sonic hedgehog (Shh) produced by ZPA represents the key mediator of the polarizing activity that regulates patterning of the limb along the
HP:0003312Abnormal form of the vertebral bodiesMP:0020010decreased bone mineral density of femurreduction in the quatitative measurment value of mineral content of bone in the long bone of the thigh
HP:0010978Abnormality of immune system physiologyMP:0011205excessive folding of visceral yolk sacthe appearance of wrinkles or folds on the surface of the visceral yolk sac
Mapped by homologous gene(Total Items:13)
HP ID HP Name MP ID MP Name Annotation
HP:0002167Neurological speech impairmentMP:0020329decreased capillary densityreduction in the number of capillaries in a given cross-sectional area of a tissue
HP:0003312Abnormal form of the vertebral bodiesMP:3000003abnormal Ebner's gland morphologyany structural anomaly of the serous salivary glands which reside adjacent to the moats surrounding the circumvallate and foliate papillae just anterior to the posterior third of the tongue, anterior to the terminal sulcus; these exocrine glands secrete l
HP:0010978Abnormality of immune system physiologyMP:0020316decreased vascular endothelial cell proliferationdecrease in the expansion rate of any vascular endothelial cell population by cell division
HP:0005019Diaphyseal thickeningMP:0013178tail necrosismorphological changes resulting from pathological death of tail tissue; usually due to irreversible damage
HP:0004493Craniofacial hyperostosisMP:0020137decreased bone mineralizationdecrease in the rate at which minerals are deposited into bone
HP:0002992Abnormality of the tibiaMP:0020137decreased bone mineralizationdecrease in the rate at which minerals are deposited into bone
HP:0002823Abnormality of the femurMP:0020137decreased bone mineralizationdecrease in the rate at which minerals are deposited into bone
HP:0002644Abnormality of pelvic girdle bone morphologyMP:0020254decreased collagen leveldecreased level of the main structural protein of the various connective tissues in animals
HP:0003103Abnormal cortical bone morphologyMP:0020137decreased bone mineralizationdecrease in the rate at which minerals are deposited into bone
HP:0006487Bowing of the long bonesMP:0020137decreased bone mineralizationdecrease in the rate at which minerals are deposited into bone
HP:0000944Abnormality of the metaphysesMP:0020137decreased bone mineralizationdecrease in the rate at which minerals are deposited into bone
HP:0001903AnemiaMP:0020316decreased vascular endothelial cell proliferationdecrease in the expansion rate of any vascular endothelial cell population by cell division
HP:0001744SplenomegalyMP:0020254decreased collagen leveldecreased level of the main structural protein of the various connective tissues in animals
Disease ID 1580
Disease ghosal hematodiaphyseal dysplasia
Case(Waiting for update.)