About: Cell surface receptor deficiencies

An Entity of Type: Concept, from Named Graph: http://dbpedia.org, within Data Space: dbpedia.org

Property	Value
dbo:wikiPageID	29894931 (xsd:integer)
dbo:wikiPageRevisionID	833646118 (xsd:integer)
dbp:wikiPageUsesTemplate	dbt:Commons_category
rdf:type	skos:Concept
rdfs:label	Cell surface receptor deficiencies (en)
skos:broader	dbc:Signal_transduction_disorders
skos:prefLabel	Cell surface receptor deficiencies (en)
prov:wasDerivedFrom	wikipedia-en:Category:Cell_surface_receptor_deficiencies?oldid=833646118&ns=14
is dbo:wikiPageWikiLink of	dbr:Pseudohypoparathyroidism dbr:Persistent_Müllerian_duct_syndrome dbr:Apert_syndrome dbr:Donnai–Barrow_syndrome dbr:Pseudopseudohypoparathyroidism dbr:Crouzon_syndrome dbr:Robinow_syndrome dbr:Congenital_amegakaryocytic_thrombocytopenia dbr:Congenital_hypothyroidism dbr:Antley–Bixler_syndrome dbr:Loeys–Dietz_syndrome dbr:Pfeiffer_syndrome dbr:Jansen's_metaphyseal_chondrodysplasia dbr:Achondroplasia dbr:Achondroplasia_in_children dbr:Familial_hypocalciuric_hypercalcemia dbr:Cenani–Lenz_syndactylism dbr:Familial_male-limited_precocious_puberty dbr:Hereditary_hemorrhagic_telangiectasia dbr:Hypochondroplasia dbr:ABCD_syndrome dbr:Aarskog–Scott_syndrome dbr:Juvenile_polyposis_syndrome dbr:Kallmann_syndrome dbr:Laron_syndrome dbr:Leber_congenital_amaurosis dbr:Jackson–Weiss_syndrome dbr:X-linked_severe_combined_immunodeficiency dbr:XX_gonadal_dysgenesis dbr:Nevoid_basal-cell_carcinoma_syndrome dbr:Short-limb_skeletal_dysplasia_with_severe_combined_immunodeficiency dbr:Muenke_syndrome dbr:Thanatophoric_dysplasia
is dcterms:subject of	dbr:Pseudohypoparathyroidism dbr:Persistent_Müllerian_duct_syndrome dbr:Apert_syndrome dbr:Donnai–Barrow_syndrome dbr:Pseudopseudohypoparathyroidism dbr:Crouzon_syndrome dbr:Robinow_syndrome dbr:Congenital_amegakaryocytic_thrombocytopenia dbr:Congenital_hypothyroidism dbr:Antley–Bixler_syndrome dbr:Loeys–Dietz_syndrome dbr:Pfeiffer_syndrome dbr:Jansen's_metaphyseal_chondrodysplasia dbr:Achondroplasia dbr:Achondroplasia_in_children dbr:Familial_hypocalciuric_hypercalcemia dbr:Cenani–Lenz_syndactylism dbr:Familial_male-limited_precocious_puberty dbr:Hereditary_hemorrhagic_telangiectasia dbr:Hypochondroplasia dbr:ABCD_syndrome dbr:Aarskog–Scott_syndrome dbr:Juvenile_polyposis_syndrome dbr:Kallmann_syndrome dbr:Laron_syndrome dbr:Leber_congenital_amaurosis dbr:Jackson–Weiss_syndrome dbr:X-linked_severe_combined_immunodeficiency dbr:XX_gonadal_dysgenesis dbr:Nevoid_basal-cell_carcinoma_syndrome dbr:Short-limb_skeletal_dysplasia_with_severe_combined_immunodeficiency dbr:Muenke_syndrome dbr:Thanatophoric_dysplasia