Phenotypes for disease #04473 (HRTFDS (Hartsfield syndrome (HRTFDS)), OMIM:615465)

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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     
0000139241 Holoprosencephaly (HPE) spectrum disorderslobar HPE (Lobar), HP:0001360, HP:0006870; corpus callosum (parzial Agenesia), HP:0001273; ectrodactyly spectrum disorders (Foot/ Right/Left), HP:0100257, HP:0001839; abnormal genitalia (Micropenis, Cryptorchidism), HP:0000811, HP:0000054, HP:0000028; central diabetes insipidus, HP:0000863; developmental delay/intellectual disability (mild), HP:0012758, HP:0001249 - - Isolated (sporadic) 12y - - - - Lucia Micale 00174403
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