Phenotypes for disease #01645 (ALMS (Alstrom syndrome (ALMS)), OMIM:203800)

9 entries on 1 page. Showing entries 1 - 9.
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Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

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Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

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Owner     

Individual ID     
0000052835 Visual loss (HP:0000572), Photophobia (HP:0000613), Pendular nystagmus (HP:0012043), - - Familial, autosomal recessive - - - - - Pieter Klap 00073166
0000060592 Alstrom syndrome (OMIM:203800) - - Familial, autosomal recessive - - - - - Daniel Trujillano 00081023
0000254045 (+) Renal insufficiency,(+) Hearing impairment,(+) Depressivity,(+) Hepatic steatosis,(+) Obesity,(+) Dilated cardiomyopathy,(+) Type II diabetes mellitus,(+) Retinitis / Sister cardiomyopathy at 23 yrs also RP, hearing loss, kidney and liver problems. - - Familial, autosomal recessive 51y - - - - Andreas Laner 00358830
0000257225 - Usher syndrome Alström syndrome Familial, autosomal recessive - - - - - Barbara Vona 00361833
0000257227 - Usher syndrome Alström syndrome Familial, autosomal recessive - - - - - Barbara Vona 00361835
0000257229 - Usher syndrome Alström syndrome Familial, autosomal recessive - - - - - Barbara Vona 00361837
0000279512 obesity (HP:0001513), insulin resistance (HP:0000855), sensorineural hearing loss (HP:0000407), renal insufficiency (HP:0000083), hypothyroidism (HP:0000821) diabetes Alstrom syndrome Familial, autosomal dominant 30y 30y 10y Diabetes mellitus HP:0000819 - Ming Zhong 00385698
0000326757 Photophobia HP:0000613, Reduced visual acuity HP:0007663, Color vision defect HP: 0000551, Acanthosis nigricans HP:0000956, Abnormality of retinal pigmentation HP:0007703 Cone rod dystrophy # 203800 Familial, autosomal recessive 06y 13y 06y - - Rocio Villafuerte-de la Cruz 00436611
0000346128 see paper; ..., abnormal visual electrophysiology; abnormal eye physiology; abnormal retinal morphology; abnormality of vision cone dysfunction syndrome - Unknown - - - - - Johan den Dunnen 00457669
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