Phenotype #0000058468

Individual ID 00078700
Associated disease CISS
Phenotype details contraction of oropharyngeal muscles (HP:?), feeding difficulties (HP:0011968), camptodactyly (HP:0012385), cyanosis (HP:0000961), swallowing difficulties (HP:0002015), full cheeks (HP:0000293), no foot anomalies (-HP:?), highly arched palate (HP:0002705), depressed nasal bridge (HP:0005280), no cold-induced sweating (-HP:?), no scoliosis (-HP:0002650), joint contractures (HP:0001371), no psychomotor retardation (-HP:0001263); feeding problems (HP:0011968); flat nasal bridge (HP:0005280); no scoliosis (-HP:0002650); camptodactyly (HP:0012385); full cheeks (HP:0000293); large joints (HP:0005781); cyanosis (HP:0000961); high palate (HP:0000218); poor swallowing (HP:0002015); no cold induced sweating (-HP:0025278)
Diagnosis/Initial -
Inheritance Familial, autosomal recessive
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis 00y06m
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Jamie Zeegers
Database submission license No license selected
Created by Jamie Zeegers
Date created 2016-07-21 13:55:10 +02:00 (CEST)
Date last edited 2020-04-07 11:38:19 +02:00 (CEST)

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