Phenotypes for disease #01290 (KCS2 (Kenny-Caffey syndrome, type 2), OMIM:127000)

2 entries on 1 page. Showing entries 1 - 2.
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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

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Owner     

Individual ID     
0000342078 Abnormality of the face, microdontia of primary teeth, high hypermetropia, astigmatism, fully accommodative esotropia, strabismus, short stature, relative macrocephaly, pectus carinatum, thoracic scoliosis, thickened cortex of long bones, stenosis of the medullary cavity of the long bones, slender long bones, delayed skeletal maturation, thin skin, sparse scalp hair, sparse eyebrows, nail dysplasia,high pitched voice, hypernasal speech, pulmonary hypoplasia, anemia, thrombocytosis, reduced circulating growth hormone concentration, decreased response to growth hormone stimulation test - - Familial, autosomal recessive - - - - - Frederike Leonie Harms 00453415
0000342079 Abnormality of the face, high hypermetropia, astigmatism, fully accommodative esotropia, short stature, dolichocephaly, thickened cortex of long bones, stenosis of the medullary cavity of the long bones, delayed skeletal maturation, hypermelanotic macule, sparse scalp hair, sparse eyebrows, nail dysplasia, high pitched voice, nasal speech, micropenis, cryptorchidism, anemia, thrombocytosis - - Familial, autosomal recessive - - - - - Frederike Leonie Harms 00453416
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