Phenotypes for disease #01716 (C1SD (complement component c1r/c1s deficiency (C1SD)), OMIM:216950)

3 entries on 1 page. Showing entries 1 - 3.
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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000128956 Dandy-Walker malformation (HP:0001305), molar-tooth sign (HP:0002419), developmental delay (HP:0001263), microcephaly (HP:0000252), cleft upper lip (HP:0000204), natal tooth (HP:0000695), hamartoma of tongue (HP:0011802), microretrognathia (HP:0000308), postaxial polydactyly (HP:0100259), cryptorchidism (HP:0000028), patent ductus arteriosis (HP:0001643); retinal coloboma (HP:0000480), hypotonia (HP:0001290) - Orofaciodigital syndrome type 14 Familial, autosomal recessive - - <00y <0y - Nicole Boczek 00163842
0000309995 Proband presenting with a LES phenotype - - Familial - 03y - - - Christian Drouet 00418696
0000325448 Proband presenting with a complete C1s and C1r deficiency, developing seizure, fever, unilateral sacroileitis and ANA+ at age 16y - 13y Familial - - - - - Christian Drouet 00435252
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