Phenotypes for disease #02945 (NFTC (Tumoral calcinosis, familial, normophosphatemic), OMIM:610455)

2 entries on 1 page. Showing entries 1 - 2.
Legend   How to query  

AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000290715 Retinopathy of prematurity: HP:0500049: Subcutaneous nodule HP:0001482: Edema HP:0000969: Erythema HP:0010783: Gingivitis HP:0000230 - Normophosphatemic familial tumoral calcinosis Familial, autosomal recessive 06y 06y 06y Retinopathy of prematurity: HP:0500049: Subcutaneous nodule HP:0001482: Edema HP:0000969: Erythema HP:0010783: Gingivitis HP:0000230 - Litika Vermani 00397591
0000302060 Retinopathy of prematurity (HP:0500049), Subcutaneous calcification (HP:0007618), Edema (HP:0000969), Erythema (HP:0010783), Abnormal pigmentation of the oral mucosa (HP:0100669), Gingivitis (HP:0000230) Normophosphatemic Familial Tumoral Calcinosis Normophosphatemic Familial Tumoral Calcinosis Familial, autosomal recessive 06y 06y 06y 06 - Litika Vermani 00397592
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.